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Items 1 to 100 of about 311
1. Milisavljevic D, Zivic M, Radovanović Z, Stankovic P: Severe dyspnea as atypical presenting symptom of Madelung's disease. Hippokratia; 2010 Apr;14(2):133-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Severe dyspnea as atypical presenting symptom of Madelung's disease.
  • Madelung's disease (benign symmetrical lipomatosis) is a rare disease of unknown etiology manifesting as symmetric abnormal deposits of adipose tissue in the head, neck and upper trunk.
  • We report a case of a 58-year-old man with a long lasting Madelungs disease in whom progressive fatty tissue accumulation caused a severe inspiratory dyspnea as atypical presenting symptom.
  • The etiopathogenetic, clinico-diagnostic and therapeutic aspects of this rare disease are discussed.
  • Due to its progressive but not so easily predictable enlarging behavior Madelung's disease has not only aesthetic but also functional and sometimes life threatening consequences which need to be treated.

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  • [Cites] AANA J. 2006 Aug;74(4):281-4 [16918119.001]
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  • (PMID = 20596272.001).
  • [ISSN] 1790-8019
  • [Journal-full-title] Hippokratia
  • [ISO-abbreviation] Hippokratia
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Greece
  • [Other-IDs] NLM/ PMC2895283
  • [Keywords] NOTNLM ; Launois-Bensaude syndrome / Madelung's disease / benign symmetrical lipomatosis
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2. Fonseca VA, Alves C, Marques H, Camacho E, Saraiva AP: Madelung's disease as a rare cause of obstructive sleep apnea. J Bras Pneumol; 2009 Oct;35(10):1053-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Madelung's disease as a rare cause of obstructive sleep apnea.
  • Madelung's disease, or multiple symmetric lipomatosis, is a rare disease, characterized by accumulation of unencapsulated fat, generally located symmetrically around the neck and shoulders.
  • Here, we present the case of a patient with diffuse lipomatosis accompanied by obstructive sleep apnea due to cervical involvement and facial deformity, which made it necessary to use nasal pillows for ventilation.
  • The patient was hospitalized with a diagnosis of pneumonia and required noninvasive ventilation due to severe hypercapnia.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / complications. Sleep Apnea, Obstructive / etiology

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  • (PMID = 19918637.001).
  • [ISSN] 1806-3756
  • [Journal-full-title] Jornal brasileiro de pneumologia : publicaça̋o oficial da Sociedade Brasileira de Pneumologia e Tisilogia
  • [ISO-abbreviation] J Bras Pneumol
  • [Language] eng; por
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Brazil
  • [Number-of-references] 23
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3. Tekin A, Ogetman Z: Central form of multiple symmetric lipomatosis: a case report. Cases J; 2009;2:8427

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Central form of multiple symmetric lipomatosis: a case report.
  • Multiple symmetric lipomatosis (also known as Madelung's disease, Launois-Bensaude syndrome or benign symmetric lipomatosis) is a rare disease, the etiology of which is unknown.
  • Multiple, symmetric, non-encapsulated lipomatous masses on the face, neck, upper arms, and upper trunk are typical in most cases.
  • Five out of the 200 cases reported in the literature were the distal form of the disease; the rest were proximal.
  • We describe, for the first time, a central form of the disease, simultaneously involving the lower trunk, arms and upper legs.

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  • [Cites] Clin Exp Rheumatol. 2008 Mar-Apr;26(2):351-3 [18565262.001]
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  • (PMID = 19918431.001).
  • [ISSN] 1757-1626
  • [Journal-full-title] Cases journal
  • [ISO-abbreviation] Cases J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2769441
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4. Sharma R, Priyadarshi RN, Seith A: Shoulder girdle lipomatosis. Singapore Med J; 2009 Sep;50(9):e315-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Shoulder girdle lipomatosis.
  • Shoulder girdle lipomatosis is an extremely rare condition, with unique clinical and imaging features.
  • We report shoulder girdle lipomatosis in a 46-year-old man who presented with a gradual soft tissue enlargement in his left shoulder.
  • We discuss the magnetic resonance imaging features of this disease and the approach to accurate diagnosis.
  • A review of the clinical and radiological features of shoulder girdle lipomatosis is also presented.
  • [MeSH-major] Lipomatosis / diagnosis. Shoulder
  • [MeSH-minor] Humans. Lipectomy / methods. Lipoma / diagnosis. Magnetic Resonance Imaging / methods. Male. Middle Aged. Treatment Outcome

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  • (PMID = 19787158.001).
  • [ISSN] 0037-5675
  • [Journal-full-title] Singapore medical journal
  • [ISO-abbreviation] Singapore Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Singapore
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5. Hirose A, Okada Y, Morita E, Tanaka Y: Benign symmetric lipomatosis associated with alcoholism. Intern Med; 2006;45(17):1001-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign symmetric lipomatosis associated with alcoholism.
  • A 46-year-old man was diagnosed as having benign symmetric lipomatosis (BSL) based on the grotesque physical examination findings and subcutaneous fat tissue biopsy.
  • [MeSH-major] Alcoholism / complications. Lipomatosis, Multiple Symmetrical / etiology

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  • (PMID = 17016000.001).
  • [ISSN] 1349-7235
  • [Journal-full-title] Internal medicine (Tokyo, Japan)
  • [ISO-abbreviation] Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Adiponectin
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6. Jeong IH, Maeng YH: Gastric lipomatosis. J Gastric Cancer; 2010 Dec;10(4):254-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Gastric lipomatosis.
  • Gastric lipomatosis is an extremely rare condition.
  • Pathology findings confirmed a gastric lipomatosis with multiple gastric ulcerations and extensive disruptions of the muscular layers.
  • This case and reports of other gastric lipomatosis cases indicate that CT should be used to characterize large submucosal masses because CT can show the specific nature and extent of the disease.
  • We believe that surgical treatment is the most appropriate treatment for symptomatic gastric lipomatosis that shows extensive gastric involvement, or when there are multiple gastric lipomas.

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  • (PMID = 22076194.001).
  • [ISSN] 2093-5641
  • [Journal-full-title] Journal of gastric cancer
  • [ISO-abbreviation] J Gastric Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC3204505
  • [Keywords] NOTNLM ; Gastrectomy / Lipomatosis / Stomach neoplasms
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7. López Sousa M, Varela Iglesias J, Bouzón Alejandro M, Lojo Rodríguez M, Pérez Muñuzuri A, Fernández Lorenzo JR: [Encephalocraniocutaneous lipomatosis (Haberland syndrome) with bilateral ocular damage]. An Pediatr (Barc); 2007 Jun;66(6):619-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Encephalocraniocutaneous lipomatosis (Haberland syndrome) with bilateral ocular damage].
  • [Transliterated title] Lipomatosis encefalocraneocutánea (síndrome de Haberland) con afectación ocular bilateral.
  • Encephalocraniocutaneous lipomatosis, or Haberland syndrome, is an unusual form of neurocutaneous syndrome.
  • Clinically, this syndrome is characterized by unilateral lipomatous hamartomas on the scalp and face, ocular damage and ipsilateral malformations of the central nervous system.
  • The differential diagnoses with other neurocutaneous mosaicisms such as Delleman, Goltz, Goldenhar or Proteus syndrome may entail some degree of difficulty due to overlapping features.
  • We report a case of Haberland syndrome in a neonate with bilateral ocular damage, illustrating the wide heterogeneity of this syndrome.
  • [MeSH-major] Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Eye Abnormalities. Humans. Infant, Newborn. Male

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  • (PMID = 17583626.001).
  • [ISSN] 1695-4033
  • [Journal-full-title] Anales de pediatría (Barcelona, Spain : 2003)
  • [ISO-abbreviation] An Pediatr (Barc)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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8. Lopez-Ceres A, Aguilar-Lizarralde Y, Villalobos Sánchez A, Prieto Sánchez E, Valiente Alvarez A: Benign symmetric lipomatosis of the tongue in Madelung's disease. J Craniomaxillofac Surg; 2006 Dec;34(8):489-93
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign symmetric lipomatosis of the tongue in Madelung's disease.
  • INTRODUCTION: Madelung's disease is characterized by benign, non-encapsulated accumulations of fat in a symmetrical manner.
  • Although rare, symmetrical lipomatosis involving the tongue exclusively has been previously reported.
  • Here another case is presented of Madelung's disease involving the tongue.
  • CASE REPORT: A 57-year-old woman was referred with the diagnosis of Madelung's disease, with slight difficulty in swallowing, dysarthria and dyspnoea while sleeping due to tongue swelling.
  • DISCUSSION: Lipomas in Madelung's disease are characterized by multiplicity, non-encapsulation and invasiveness.
  • The aetiology of benign symmetrical lipomatosis is still unknown.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / pathology. Lipomatosis, Multiple Symmetrical / surgery. Macroglossia / pathology. Macroglossia / surgery

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  • (PMID = 17157517.001).
  • [ISSN] 1010-5182
  • [Journal-full-title] Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
  • [ISO-abbreviation] J Craniomaxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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9. Stopar T, Novak Jankovic V, Casati A: Four different airway-management strategies in patient with Launois-Bensaude syndrome or Madelung's disease undergoing surgical excision of neck lipomatosis with a complicated postoperative course. J Clin Anesth; 2005 Jun;17(4):300-3
Genetic Alliance. consumer health - Madelung's disease.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Four different airway-management strategies in patient with Launois-Bensaude syndrome or Madelung's disease undergoing surgical excision of neck lipomatosis with a complicated postoperative course.
  • Launois-Bensaude syndrome, otherwise known as Madelung's disease, is a rare disorder characterized by fatty accumulations of the upper trunk, neck and head, causing serious cosmetic deformity and neck immobility.
  • We report a case of a patient with Launois-Bensaude syndrome who required 4 different airway management strategies during his hospitalization for postoperative complications after an elective surgical excision of a severe neck lipomatosis.
  • Anesthesiologists who treat patients with Madelung's disease should be aware of 2 major problems: difficult airway and increased frequency of postoperative bleeding.
  • [MeSH-major] Intubation, Intratracheal / methods. Laryngeal Masks. Lipomatosis, Multiple Symmetrical / surgery. Postoperative Hemorrhage / etiology

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  • (PMID = 15950858.001).
  • [ISSN] 0952-8180
  • [Journal-full-title] Journal of clinical anesthesia
  • [ISO-abbreviation] J Clin Anesth
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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10. Hasegawa T, Matsukura T, Ikeda S: Mesotherapy for benign symmetric lipomatosis. Aesthetic Plast Surg; 2010 Apr;34(2):153-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mesotherapy for benign symmetric lipomatosis.
  • BACKGROUND: Benign symmetric lipomatosis, also known as Madelung disease, is a rare disorder characterized by fat distribution around the shoulders, arms, and neck in the context of chronic alcoholism.
  • However, reports describing conservative therapeutic measures for lipomatosis are rare.
  • METHODS: The authors present the case of a 42-year-old man with a diagnosis of benign symmetric lipomatosis who had multiple, large, symmetrical masses in his neck.
  • RESULTS: The patient's lipomatosis improved in response to the injections, and he achieved good cosmetic results.
  • CONCLUSIONS: Intralesional injection, termed mesotherapy, using phosphatidylcholine is a potentially effective therapy for benign symmetric lipomatosis that should be reconsidered as a therapeutic option for this disease.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / drug therapy. Phosphatidylcholines / therapeutic use

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  • [CommentIn] Aesthetic Plast Surg. 2011 Apr;35(2):278-80 [20835822.001]
  • (PMID = 19488808.001).
  • [ISSN] 1432-5241
  • [Journal-full-title] Aesthetic plastic surgery
  • [ISO-abbreviation] Aesthetic Plast Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Phosphatidylcholines
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11. Schoffer K, Grant I: Multiple lipomas, alcoholism, and neuropathy: Madelung's disease or MERRF? Muscle Nerve; 2006 Jan;33(1):142-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple lipomas, alcoholism, and neuropathy: Madelung's disease or MERRF?
  • We report a 51-year-old alcoholic man with a 10-year history of cervical lipomas and progressive symmetrical sensory neuropathy, initially diagnosed with Madelung's disease, an idiopathic syndrome often attributed to chronic alcoholism.
  • This case demonstrates how the varied terminology for this syndrome has resulted in a lack of consistent recognition and assessment for mitochondrial cytopathy.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis. Lipomatosis, Multiple Symmetrical / genetics. MERRF Syndrome / diagnosis. MERRF Syndrome / genetics. RNA, Transfer, Lys / genetics
  • [MeSH-minor] Alcoholic Neuropathy / diagnosis. Alcoholism / diagnosis. Humans. Lipoma / diagnosis. Male. Middle Aged. Muscle, Skeletal / ultrastructure. Mutation. RNA / genetics

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  • (PMID = 16007676.001).
  • [ISSN] 0148-639X
  • [Journal-full-title] Muscle & nerve
  • [ISO-abbreviation] Muscle Nerve
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / RNA, Transfer, Lys; 0 / RNA, mitochondrial; 63231-63-0 / RNA
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12. Poggi G, Moro G, Teragni C, Delmonte A, Saini G, Bernardo G: Scrotal involvement in Madelung disease: clinical, ultrasound and MR findings. Abdom Imaging; 2006 Jul-Aug;31(4):503-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Scrotal involvement in Madelung disease: clinical, ultrasound and MR findings.
  • Multiple symmetrical lipomatosis, also known as Madelung disease, Launois-Bensaude syndrome, and benign symmetrical lipomatosis, is an uncommon disease that is characterized by the presence of multiple and symmetrical deposits of nonencapsulated adipose tissue in the neck, upper trunk, arms, and legs.
  • [MeSH-major] Genital Diseases, Male / diagnosis. Lipomatosis, Multiple Symmetrical / diagnosis. Scrotum / pathology

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  • (PMID = 16447078.001).
  • [ISSN] 0942-8925
  • [Journal-full-title] Abdominal imaging
  • [ISO-abbreviation] Abdom Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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13. Chen XM, Li WY, Ni DF, Wei BJ, Xu CX, Gao ZQ, He L, Chen YN: [Diagnosis and treatment of Madelung's disease]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Jul;41(7):524-7
Genetic Alliance. consumer health - Madelung's disease.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Diagnosis and treatment of Madelung's disease].
  • OBJECTIVE: To review the characteristics of Madelung's disease which is rare and unfamiliar to clinicians and to find the method of diagnosis and treatment.
  • METHODS: Detailed clinical data of 7 patients with Madelung's disease were reviewed and analyzed.
  • These 3 patients were associated with sleep apnea syndrome simultaneously.
  • Another one patient was accompanied by autonomic nervous system disease only.
  • CONCLUSIONS: Madelung's disease is characterized by massive accumulation of nonencapsulated subcutaneous fat mainly located symmetrically in the neck.
  • It may be associated with some internal diseases.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis. Lipomatosis, Multiple Symmetrical / surgery

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  • (PMID = 17007380.001).
  • [ISSN] 1673-0860
  • [Journal-full-title] Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
  • [ISO-abbreviation] Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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14. Ali S, Kishore A: Dysphagia and obstructive sleep apnoea in Madelung's disease. J Laryngol Otol; 2007 Apr;121(4):398-400
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Dysphagia and obstructive sleep apnoea in Madelung's disease.
  • Madelung's disease is a benign disorder characterized by the presence of lipomata in the head and neck areas.
  • [MeSH-major] Deglutition Disorders / etiology. Lipomatosis, Multiple Symmetrical / complications. Sleep Apnea, Obstructive / etiology

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  • (PMID = 17164023.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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15. Ettl T, Gaumann A, Ehrenberg R, Reichert TE, Driemel O: Encapsulated lipomas of the tongue in benign symmetric lipomatosis. J Dtsch Dermatol Ges; 2009 May;7(5):441-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Encapsulated lipomas of the tongue in benign symmetric lipomatosis.
  • Benign symmetric lipomatosis (Madelung disease) is a rare disorder of unknown etiology characterized by diffuse growth of unencapsulated lipomas predominantly in the head, neck and shoulder region.
  • A 49-year-old man with alcoholic liver cirrhosis presented with an 11-year history of benign symmetric lipomatosis complaining of increasing dysphagia, dysarthria and hoarseness.
  • [MeSH-major] Lipomatosis / pathology. Lipomatosis / surgery. Tongue Diseases / pathology. Tongue Diseases / surgery

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  • (PMID = 19192164.001).
  • [ISSN] 1610-0387
  • [Journal-full-title] Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
  • [ISO-abbreviation] J Dtsch Dermatol Ges
  • [Language] eng; ger
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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16. Jurić M, Carapina M: A case repot of Madelung's disease in a 69 years old man. Coll Antropol; 2009 Dec;33 Suppl 2:169-71
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case repot of Madelung's disease in a 69 years old man.
  • Madelung's disease is an extremely rare disorder of unknown etiology.
  • A 69-old patient with developed symptoms of Madelung's disease with a 12-years history is described in this study.
  • Although the Madelung's disease can be diagnosed right after detailed clinical examination, this study pointed out possible diagnostic and therapeutic mistakes when a physician in a differentiation of symmetrical neck and shoulder swellings doesn't consider the possibility of diagnosing a Madelung's disease.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical
  • [MeSH-minor] Aged. Bosnia and Herzegovina. Diagnosis, Differential. Diagnostic Errors. Goiter / diagnosis. Heart Failure / diagnosis. Humans. Male

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  • (PMID = 20120407.001).
  • [ISSN] 0350-6134
  • [Journal-full-title] Collegium antropologicum
  • [ISO-abbreviation] Coll Antropol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Croatia
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17. Gdynia HJ, Sperfeld AD, Knirsch U, Homberg V, Rosenbohm A, Müller-Höcker J, Ludolph AC, Hanemann CO: Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regions. Eur J Med Res; 2006 Dec 14;11(12):545-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regions.
  • Benign symmetric lipomatosis, also called Madelung's disease, is characterized by lipomata and fatty infiltrations.
  • We report a 55 year old male suffering from benign symmetric lipomatosis with associated axonal neuropathy and hyperlipoproteinemia.
  • [MeSH-major] Axons / physiology. Hyperlipoproteinemias / genetics. Lipomatosis, Multiple Symmetrical / genetics. Peripheral Nervous System Diseases / genetics. RNA / genetics. RNA, Transfer / genetics

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  • [CommentOn] Eur J Med Res. 2006 Apr 28;11(4):174-7 [16720284.001]
  • (PMID = 17182368.001).
  • [ISSN] 0949-2321
  • [Journal-full-title] European journal of medical research
  • [ISO-abbreviation] Eur. J. Med. Res.
  • [Language] eng
  • [Publication-type] Case Reports; Comment; Letter
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / RNA, mitochondrial; 63231-63-0 / RNA; 9014-25-9 / RNA, Transfer
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18. Guilemany JM, Romero E, Blanch JL: An aesthetic deformity: Madelung's disease. Acta Otolaryngol; 2005 Mar;125(3):328-30
Genetic Alliance. consumer health - Madelung's disease.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An aesthetic deformity: Madelung's disease.
  • Madelung's disease, also known as benign symmetric lipomatosis, multiple symmetrical lipomatosis or Lanois-Bensaude syndrome, consists of growth of fatty masses predominantly on the face, neck, shoulders, upper thorax and arms.
  • These painless and symmetrical fatty deposits can cause important aesthetic changes in these patients.
  • The aetiology of Madelung's disease remains unknown, although approximately = 60% of affected patients are clinically overweight and there is an intimate association with chronic alcohol abuse.
  • We report an unusual case of Madelung's disease in a 52-year-old male.
  • The patient remains well and disease-free after 12 months of postoperative follow-up.
  • [MeSH-major] Esthetics. Lipomatosis, Multiple Symmetrical / surgery

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  • (PMID = 15966707.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Norway
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19. Linares Torres P, Castañón López C, Llano Alonso C, Alvarez Posadilla M, Vivas Alegre S, Espinel Díez J, Ribas Arino MT: [Association of adenocarcinoma of esophagus and breast cancer in a male with Madelung' disease]. An Med Interna; 2006 Mar;23(3):133-5
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  • [Title] [Association of adenocarcinoma of esophagus and breast cancer in a male with Madelung' disease].
  • [Transliterated title] Asociación de adenocarcinoma de esófago y cáncer de mama en un varón con enfermedad de Madelung.
  • We report a case of adenocarcinoma of the esophagus in a man diagnosed of benign symmetrical lipomatosis (Madelung' disease), who had received adjuvant radiotherapy three years before for breast cancer.
  • [MeSH-major] Adenocarcinoma / complications. Breast Neoplasms, Male / complications. Carcinoma, Ductal, Breast / complications. Esophageal Neoplasms / complications. Lipomatosis, Multiple Symmetrical / complications. Neoplasms, Radiation-Induced / etiology. Neoplasms, Second Primary / etiology. Radiotherapy, Adjuvant / adverse effects


20. Goetze S, Hommann M, Elsner P, Kaatz M: Induction of benign symmetric lipomatosis (Launois-Bensaude syndrome) in a female patient after liver transplantation. Dermatology; 2008;216(4):337-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Induction of benign symmetric lipomatosis (Launois-Bensaude syndrome) in a female patient after liver transplantation.
  • Benign symmetric lipomatosis, also known as Madelung's disease or Launois-Bensaude syndrome, is a rare disease, the etiology of which is still unknown.
  • The presence of multiple, symmetric, nonencapsulated lipomatous masses in the face, neck, upper arms and upper trunk is typical.
  • In our case the Launois-Bensaude syndrome developed after liver transplantation in a 49-year-old female patient suffering from decompensated cirrhosis (Child-Pugh C score: 12 points).
  • As far as we know, this case is the first description of the induction of a Launois-Bensaude syndrome following liver transplantation.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / etiology. Liver Transplantation / adverse effects

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  • [Copyright] Copyright 2008 S. Karger AG, Basel.
  • (PMID = 18268407.001).
  • [ISSN] 1421-9832
  • [Journal-full-title] Dermatology (Basel, Switzerland)
  • [ISO-abbreviation] Dermatology (Basel)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Glucocorticoids; 9PHQ9Y1OLM / Prednisolone
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21. Gotovac J, Vrsalović N, Librenjak D, Milostić K, Situm M: [Lipomatosis pelvis]. Acta Med Croatica; 2007 Sep;61(4):411-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Lipomatosis pelvis].
  • [Transliterated title] Lipomatosis pelvis.
  • The article is a discussion of three cases of lipomatosis in the pelvis and of the surgical treatment undertaken in each case.
  • In all three cases, the diagnosis by ultrasound, intravenous urography and rectoscopy was confirmed by CT.
  • [MeSH-major] Lipomatosis. Pelvic Neoplasms

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  • (PMID = 18044478.001).
  • [ISSN] 1330-0164
  • [Journal-full-title] Acta medica Croatica : c̆asopis Hravatske akademije medicinskih znanosti
  • [ISO-abbreviation] Acta Med Croatica
  • [Language] hrv
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Croatia
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22. Shetty C, Avinash KR, Auluck A, Mupparapu M: Multiple symmetric lipomatosis (MSL) of neck in a child (Madelung's disease): report of a rare presentation. Dentomaxillofac Radiol; 2007 Jan;36(1):51-4
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  • [Title] Multiple symmetric lipomatosis (MSL) of neck in a child (Madelung's disease): report of a rare presentation.
  • A case of multiple symmetric lipomatosis (MSL) of neck, also known as Madelung's disease or Launois-Bensaude syndrome, is reported in an 8-year-old girl who presented with bilateral swellings in the neck.
  • Metabolic disturbances and malignant tumours have also been associated with this disorder.
  • The recognition of this disease is important as, in addition to cosmetic abnormality, it can compress the important neurovascular structures.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis
  • [MeSH-minor] Child. Diagnosis, Differential. Female. Head and Neck Neoplasms / diagnosis. Humans. Lymphangioma, Cystic / diagnosis. Mediastinum / pathology. Neck / pathology. Tomography, X-Ray Computed

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  • (PMID = 17329589.001).
  • [ISSN] 0250-832X
  • [Journal-full-title] Dento maxillo facial radiology
  • [ISO-abbreviation] Dentomaxillofac Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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23. Conroy JP: Airway management: a patient with Madelung disease. AANA J; 2006 Aug;74(4):281-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Airway management: a patient with Madelung disease.
  • The patient was diagnosed with multiple symmetric lipomatosis, better known by its eponym, Madelung disease.
  • This disease is characterized by abnormal adipose tissue growth primarily in the neck and shoulder regions.
  • [MeSH-major] Airway Obstruction / therapy. Anesthesia, General / methods. Lipomatosis, Multiple Symmetrical / surgery. Nurse Anesthetists

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  • (PMID = 16918119.001).
  • [ISSN] 0094-6354
  • [Journal-full-title] AANA journal
  • [ISO-abbreviation] AANA J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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24. Ramos S, Pinheiro S, Diogo C, Cabral L, Cruzeiro C: Madelung disease: a not-so-rare disorder. Ann Plast Surg; 2010 Jan;64(1):122-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Madelung disease: a not-so-rare disorder.
  • Madelung disease is characterized by the formation of diffuse uncapsulated lipomata in different body areas and is responsible for severe cosmetic deformities.
  • The authors make a revision of the literature on this disease and then report on the cases of Madelung disease operated between January 2003 and October 2008 at the Plastic surgery department of Coimbra University Hospital.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / surgery. Reconstructive Surgical Procedures / methods

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  • [CommentIn] Ann Plast Surg. 2010 Jun;64(6):807-8 [20489411.001]
  • (PMID = 20023459.001).
  • [ISSN] 1536-3708
  • [Journal-full-title] Annals of plastic surgery
  • [ISO-abbreviation] Ann Plast Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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25. Zhang XY, Li NY: [Madelung disease: CT and MRI findings]. Zhonghua Kou Qiang Yi Xue Za Zhi; 2007 Mar;42(3):186-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Madelung disease: CT and MRI findings].
  • OBJECTIVE: To investigate the CT and MRI manifestations of Madelung disease.
  • METHODS: The CT and MRI manifestations of 12 cases of Madelung disease were analyzed retrospectively.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis. Magnetic Resonance Imaging. Tomography, X-Ray Computed

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  • (PMID = 17565834.001).
  • [ISSN] 1002-0098
  • [Journal-full-title] Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology
  • [ISO-abbreviation] Zhonghua Kou Qiang Yi Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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26. Mayor M, Arillo A, Tiberio G: [Multiple symmetric lipomatosis: a case report]. An Sist Sanit Navar; 2006 Sep-Dec;29(3):433-7
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  • [Title] [Multiple symmetric lipomatosis: a case report].
  • [Transliterated title] Lipomatosis simétrica múltiple: a propósito de un caso.
  • We present the case of a 46 year-old man with Multiple Symmetric Lipomatosis (MSL), an infrequent disease with an unknown aetiology.
  • MSL type I disease was diagnosed.
  • The treatment of choice, the lipectomy, was performed, making it possible to obtain a substantial disease improvement, both physical and aesthetically.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / pathology

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  • (PMID = 17224944.001).
  • [ISSN] 1137-6627
  • [Journal-full-title] Anales del sistema sanitario de Navarra
  • [ISO-abbreviation] An Sist Sanit Navar
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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27. Leffler M, Kneser U, Bach AD, Kopp J, Horch RE: [Vacuum-assisted closure (V.A.C.) of disastrous wound conditions in Madelung disease]. Zentralbl Chir; 2006 Apr;131 Suppl 1:S15-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Vacuum-assisted closure (V.A.C.) of disastrous wound conditions in Madelung disease].
  • [Transliterated title] Vakuumtherapie in der Behandlung desaströser Wundverhältnisse bei Morbus Madelung.
  • INTRODUCTION: A 54 year old patient presented with a Madelung disease.
  • [MeSH-major] Lipectomy. Lipomatosis, Multiple Symmetrical / surgery. Occlusive Dressings. Surgical Flaps. Surgical Wound Dehiscence / surgery. Surgical Wound Infection / surgery

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  • (PMID = 16575638.001).
  • [ISSN] 0044-409X
  • [Journal-full-title] Zentralblatt für Chirurgie
  • [ISO-abbreviation] Zentralbl Chir
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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28. Shen CY, Ou CH, Tsao TF, Wu MC, Tyan YS: Multiple symmetric lipomatosis in two chinese patients, one typical and one unusual. Neuroradiol J; 2009 Jan 20;21(6):801-4
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  • [Title] Multiple symmetric lipomatosis in two chinese patients, one typical and one unusual.
  • Multiple symmetric lipomatosis (MSL; Madelung disease) is an uncommon disorder with diffuse multiple symmetrical unencapsulated accumulations of fat located in the neck and the upper trunk.

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  • (PMID = 24257048.001).
  • [ISSN] 1971-4009
  • [Journal-full-title] The neuroradiology journal
  • [ISO-abbreviation] Neuroradiol J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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29. Kan Y, Yao P, Xin W, Chen Q, Wang J, Yue J, Zhu J: [Recent progress on diagnosis and treatment of benign symmetric lipomatosis]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Feb;24(3):105-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Recent progress on diagnosis and treatment of benign symmetric lipomatosis].
  • OBJECTIVE: To introduce recent progress on diagnosis and treatment of benign symmetric lipomatosis (BSL).
  • We present a summary of the clinical symptoms, physical sign, diagnosis and therapeutic methods of BSL.
  • Six patients had the complication of left ventricular diastolic function changes, glucose intolerance or diabetes mellitus, chronic hepatopathy, hyperuricemia and sleep apnea syndrome in one or more.
  • Chronic alcohol addiction and typical clinical symptoms help to diagnosis BSL.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical

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  • (PMID = 20429378.001).
  • [ISSN] 1001-1781
  • [Journal-full-title] Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
  • [ISO-abbreviation] Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] Benign symmetrical lipomatosis
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30. Zuber M, Pittasch D: Benign symmetric lipomatosis (Launois-Bensaude syndrome). A rare cause of muscular weakness. Eur J Med Res; 2006 Apr 28;11(4):174-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign symmetric lipomatosis (Launois-Bensaude syndrome). A rare cause of muscular weakness.
  • She was obese and had a symmetric accumulation of fatty tissue with a bumpy structure at both arms which gave the patient a pseudoathletic appearance.
  • She suffered from benign symmetric lipomatosis (BSL), also called Launois-Bensaude syndrome (LBS), which is a rare disorder of unknown origin and poorly understood pathophysiology.
  • It is believed to be a disease of disturbed lipogenesis induced by catecholamines.
  • The syndrome is often associated with features of metabolic syndrome such as diabetes mellitus, hyperuricemia, hyperlipidemia and hypertension and is associated with polyneuropathy which is an integral part of the disease.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / complications. Muscle Weakness / etiology

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  • [CommentIn] Eur J Med Res. 2006 Dec 14;11(12):545-6 [17182368.001]
  • (PMID = 16720284.001).
  • [ISSN] 0949-2321
  • [Journal-full-title] European journal of medical research
  • [ISO-abbreviation] Eur. J. Med. Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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31. Moog U: Encephalocraniocutaneous lipomatosis. J Med Genet; 2009 Nov;46(11):721-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Encephalocraniocutaneous lipomatosis.
  • BACKGROUND: Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder of unknown aetiology.
  • It has repeatedly been discussed as a localised form of Proteus syndrome.
  • ECCL is considered to differ from Proteus syndrome in particular, but oculoectodermal syndrome is possibly a mild variant.
  • [MeSH-major] Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Diagnosis, Differential. Female. Humans. Infant. Infant, Newborn. Male. Phenotype. Proteus Syndrome / diagnosis


32. Gogălniceanu D, Trandafir D, Trandafir V, Costan VV: [The value of radical surgical treatment in benign symmetric lipomatosis]. Rev Med Chir Soc Med Nat Iasi; 2005 Jan-Mar;109(1):158-63

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [The value of radical surgical treatment in benign symmetric lipomatosis].
  • Benign symmetric lipomatosis (BSL) is a rare proliferative disorder of the adipose tissue, characterized by symmetrical fat deposits, predominantly in the neck and shoulder area, upper back and arms.
  • The followed parameters were: sex, age, heredo-collateral antecedents, associated organic diseases, the motivation of medical addressability, the sites of first lesions, the length of evolution before the admission, methods for diagnosis, number of surgical sessions necessary to extirpation of fat deposits, the results of the periodic follow-up examination.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / surgery

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  • (PMID = 16607847.001).
  • [ISSN] 0048-7848
  • [Journal-full-title] Revista medico-chirurgicală̆ a Societă̆ţ̜ii de Medici ş̧i Naturaliş̧ti din Iaş̧i
  • [ISO-abbreviation] Rev Med Chir Soc Med Nat Iasi
  • [Language] rum
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Romania
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33. Haloi AK, Ditchfield M, Penington A, Phillips R: Facial infiltrative lipomatosis. Pediatr Radiol; 2006 Nov;36(11):1159-62
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Facial infiltrative lipomatosis.
  • BACKGROUND: Although there are multiple case reports and small series concerning facial infiltrative lipomatosis, there is no composite radiological description of the condition.
  • OBJECTIVE: Radiological evaluation of facial infiltrative lipomatosis using plain film, sonography, CT and MRI.
  • MATERIALS AND METHODS: We radiologically evaluated four patients with facial infiltrative lipomatosis.
  • MRI provided better delineation of the exact extent of the process and characterization of facial infiltrative lipomatosis.
  • CONCLUSION: Facial infiltrative lipomatosis should be considered as a differential diagnosis of vascular or lymphatic malformation when a child presents with unilateral facial swelling.
  • [MeSH-major] Face / abnormalities. Lipomatosis / diagnosis. Paranasal Sinuses / pathology

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  • [Cites] J Oral Maxillofac Surg. 1987 Oct;45(10):879-83 [3309227.001]
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  • (PMID = 16953375.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] AU0V1LM3JT / Gadolinium
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34. Zhang XY, Li NY, Xiao WL: Madelung disease: manifestations of CT and MR imaging. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 May;105(5):e57-64

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Madelung disease: manifestations of CT and MR imaging.
  • OBJECTIVE: The purpose of the present study was to assess the head and neck imaging features of Madelung disease on computerized tomography (CT) and magnetic resonance imaging (MRI), delineate the effects of the fatty deposits on underlying structures, and tabulate the anatomic sites where the neck fat was deposited.
  • STUDY DESIGN: Sixteen Chinese patients with Madelung disease in our hospital were reviewed.
  • RESULTS: Cross-sectional CT showed that the excess fat was symmetric and unencapsulated, mainly deposited at the anterior or posterior subcutaneous tissue of the neck, was deep under the sternocleidomastoid and trapezius muscles, was situated in the posterior cervical triangle, and was around the salivary glands.
  • The CT and MRI can accurately diagnose the disease and exclude other soft tissue tumors.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / pathology
  • [MeSH-minor] Adipose Tissue, White / pathology. Adult. Aged. Diagnosis, Differential. Female. Humans. Lipogenesis. Lipoma / diagnosis. Magnetic Resonance Imaging. Male. Middle Aged. Neck / pathology. Obesity / diagnosis. Retrospective Studies. Soft Tissue Neoplasms / diagnosis. Tomography, Spiral Computed

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  • (PMID = 18329916.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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35. Secko M, Zehtabchi S: Complicated diffuse lipomatosis mimicking ascites. Am J Emerg Med; 2008 Mar;26(3):379.e1-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Complicated diffuse lipomatosis mimicking ascites.
  • Lipomatosis is a nonmalignant disease of unknown origin distinguished by overgrowth of nonencapsulated fatty tissue usually in the abdominal and pelvic cavities.
  • Limited cases of complicated mediastino-abdominal lipomatosis have been described in the literature.
  • We present a case of complicated diffuse lipomatosis mimicking ascites in a 65-year-old man.
  • [MeSH-major] Lipomatosis / radiography
  • [MeSH-minor] Aged. Ascites / radiography. Diagnosis, Differential. Humans. Male. Radiography, Thoracic. Tomography, X-Ray Computed

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  • (PMID = 18358964.001).
  • [ISSN] 1532-8171
  • [Journal-full-title] The American journal of emergency medicine
  • [ISO-abbreviation] Am J Emerg Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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36. López López AI, Cao Avellaneda E, Maluff Torres A, López Cubillana P, Prieto González A, Pérez Albacete M: [Kidney lipomatosis in a transplantation donor]. Actas Urol Esp; 2006 Jun;30(6):630-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Kidney lipomatosis in a transplantation donor].
  • [Transliterated title] Lipomatosis renal en donante cadáver.
  • [MeSH-major] Kidney Diseases / surgery. Kidney Transplantation. Lipomatosis / surgery

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  • (PMID = 16921842.001).
  • [ISSN] 0210-4806
  • [Journal-full-title] Actas urologicas españolas
  • [ISO-abbreviation] Actas Urol Esp
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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37. Pires Fraga MF, Mello D, Jorge D, Perin LF, Helene A: Congenital infiltrating lipomatosis. J Plast Reconstr Aesthet Surg; 2009 Dec;62(12):e561-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital infiltrating lipomatosis.
  • The congenital infiltrating lipomatosis (LCI) represents a distinct, clinical and pathological aspect of fat soft-tissue neoplasia; very few cases of which have been described in literature.
  • In this article, we describe a congenital infiltrating lipomatosis of the face in a child and discuss the diagnoses and the treatment of this disease.
  • [MeSH-major] Face / pathology. Lipomatosis / congenital. Lipomatosis / diagnosis
  • [MeSH-minor] Child, Preschool. Diagnosis, Differential. Fatal Outcome. Humans. Male. Mouth Diseases / congenital. Mouth Diseases / diagnosis. Mouth Diseases / surgery

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  • (PMID = 19124289.001).
  • [ISSN] 1878-0539
  • [Journal-full-title] Journal of plastic, reconstructive & aesthetic surgery : JPRAS
  • [ISO-abbreviation] J Plast Reconstr Aesthet Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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38. Dhawan SS, Khouzam R: Atypical mediastinal lipomatosis. Heart Lung; 2007 May-Jun;36(3):223-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical mediastinal lipomatosis.
  • To the authors' knowledge, this is only the second reported case of mediastinal lipomatosis that occurred in the absence of endogenous or exogenous steroid excess or obesity, with diffuse fatty infiltration, suspected on chest radiography and transthoracic echocardiography and confirmed by computed tomography of the chest.
  • [MeSH-major] Dyspnea / diagnosis. Dyspnea / etiology. Heart Atria / pathology. Lipomatosis / diagnosis. Mediastinal Diseases / diagnosis

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  • (PMID = 17509429.001).
  • [ISSN] 0147-9563
  • [Journal-full-title] Heart & lung : the journal of critical care
  • [ISO-abbreviation] Heart Lung
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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39. Waniczek D, Buda K, Mikusek W, Rudzki M, Klakla K, Arendt J: [Madelung's disease]. Wiad Lek; 2009;62(3):163-7
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  • [Title] [Madelung's disease].
  • Madelung's disease (Md) is a rare metabolic disorder which presents with multiple symmetrical nonencapsulated fatty masses situated mainly around the head, neck and nape.
  • The disease is progressive, relapses after removal of tissue are often observed.
  • There were no sings of disease recurrence.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis. Lipomatosis, Multiple Symmetrical / surgery

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  • (PMID = 20229712.001).
  • [ISSN] 0043-5147
  • [Journal-full-title] Wiadomości lekarskie (Warsaw, Poland : 1960)
  • [ISO-abbreviation] Wiad. Lek.
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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40. Fernández-Vozmediano J, Armario-Hita J: Benign symmetric lipomatosis (Launois-Bensaude syndrome). Int J Dermatol; 2005 Mar;44(3):236-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign symmetric lipomatosis (Launois-Bensaude syndrome).
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / pathology
  • [MeSH-minor] Adult. Female. Humans. Syndrome

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  • (PMID = 15807734.001).
  • [ISSN] 0011-9059
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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41. Gu W, Dou J, Yang G, Li J, Ba J, Lu Z, Mu Y, Lu J: The endocrine and metabolic evaluation of benign symmetrical lipomatosis: a case report and literature review. Neuro Endocrinol Lett; 2010;31(4):446-50

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The endocrine and metabolic evaluation of benign symmetrical lipomatosis: a case report and literature review.
  • OBJECTIVE: Benign symmetrical lipomatosis (BSL) is a rare disease characterized by the presence of multiple, symmetric and nonencapsulated fat masses.
  • However the etiology of this disease is still unclarified.
  • We also discussed the clinical manifestation, etiology, diagnosis and treatment for BSL.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical

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  • (PMID = 20802440.001).
  • [ISSN] 0172-780X
  • [Journal-full-title] Neuro endocrinology letters
  • [ISO-abbreviation] Neuro Endocrinol. Lett.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Sweden
  • [Chemical-registry-number] Benign symmetrical lipomatosis
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42. Woodhouse JB, Delahunt B, English SF, Fraser HH, Ferguson MM: Testicular lipomatosis in Cowden's syndrome. Mod Pathol; 2005 Sep;18(9):1151-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Testicular lipomatosis in Cowden's syndrome.
  • Cowden's syndrome is either familial or sporadic and is associated with the predominantly postpubertal development of a variety of cutaneous, stromal and visceral neoplasms.
  • The syndrome is associated with mutations of the PTEN gene and is closely related to Bannayan's syndrome in which macrocephaly and benign tumors, especially lipomas and hemangiomas are pathognomic.
  • In PTEN knockout mice testicular tumors have been reported and for this reason we felt it prudent to examine the testes of our patients with genetically proven Cowden's syndrome.
  • The high incidence of testicular lipomatosis in our adult subjects suggests this to be an important diagnostic criterion for Cowden's syndrome.
  • [MeSH-major] Hamartoma Syndrome, Multiple / complications. Lipomatosis / etiology. Testicular Diseases / etiology
  • [MeSH-minor] Adipocytes / cytology. Adipocytes / metabolism. Adolescent. Adult. Biomarkers. Humans. Immunohistochemistry. Male. Middle Aged. Ultrasonography

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  • (PMID = 15920539.001).
  • [ISSN] 0893-3952
  • [Journal-full-title] Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
  • [ISO-abbreviation] Mod. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers
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43. Xu Y, Liu RL, Zhang ZH, Zhao WM, Yang QC: Renal replacement lipomatosis. Eur Surg Res; 2006;38(4):385-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Renal replacement lipomatosis.
  • We report a relatively rare case of renal replacement lipomatosis presenting as a renal mass.
  • The differential diagnosis before surgery was squamous cell carcinoma, teratoma, or angiomyolipoma of the kidney.
  • The case was initially misdiagnosed, because we had no experience with this disease.
  • After mass exploration, histological examination confirmed the diagnosis of renal replacement lipomatosis.
  • [MeSH-major] Kidney Diseases / diagnosis. Lipomatosis / diagnosis

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  • [Copyright] Copyright 2006 S. Karger AG, Basel.
  • (PMID = 16837809.001).
  • [ISSN] 0014-312X
  • [Journal-full-title] European surgical research. Europäische chirurgische Forschung. Recherches chirurgicales européennes
  • [ISO-abbreviation] Eur Surg Res
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
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44. Khan M, Nazir SS, Ahangar S, Farooq Qadri SJ, Salroo NA: Total renal replacement lipomatosis. Int J Surg; 2010;8(4):263-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Total renal replacement lipomatosis.
  • Renal replacement lipomatosis can be defined as the proliferation of fibrofatty tissue which subsequently replaces the renal parenchyma.
  • There may be moderate replacement of renal tissue by fat as in renal sinus lipomatosis or in severe cases the whole of the renal parenchyma may be replaced by fat and is referred to as renal replacement lipomatosis.
  • Herein we report a case of total renal replacement lipomatosis.
  • [MeSH-major] Kidney Diseases / pathology. Kidney Diseases / surgery. Lipomatosis / pathology. Lipomatosis / surgery

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  • [Copyright] Copyright (c) 2010 Surgical Associates Ltd. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20211279.001).
  • [ISSN] 1743-9159
  • [Journal-full-title] International journal of surgery (London, England)
  • [ISO-abbreviation] Int J Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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45. Moog U, Jones MC, Viskochil DH, Verloes A, Van Allen MI, Dobyns WB: Brain anomalies in encephalocraniocutaneous lipomatosis. Am J Med Genet A; 2007 Dec 15;143A(24):2963-72
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Brain anomalies in encephalocraniocutaneous lipomatosis.
  • Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder characterized by ocular anomalies, skin lesions, and CNS anomalies.
  • We report on four new patients with this syndrome.
  • Thirty-three of 52 patients showed intracranial lipomas, frequently of cerebello-pontine location, and/or spinal lipomatosis.
  • [MeSH-major] Brain / abnormalities. Brain Diseases / diagnosis. Eye Diseases / diagnosis. Lipomatosis / complications. Neurocutaneous Syndromes / diagnosis
  • [MeSH-minor] Abnormalities, Multiple / diagnosis. Adolescent. Child. Child, Preschool. Female. Humans. Infant. Magnetic Resonance Imaging / methods. Male. Syndrome


46. Sofiatti A, Cirto AG, Arnone M, Romiti R, Santi C, Leite C, Sotto M: Encephalocraniocutaneous lipomatosis: clinical spectrum of systemic involvement. Pediatr Dermatol; 2006 Jan-Feb;23(1):27-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Encephalocraniocutaneous lipomatosis: clinical spectrum of systemic involvement.
  • Encephalocraniocutaneous lipomatosis is a rare neurocutaneous syndrome with involvement of ectomesodermal tissues.
  • Unilateral lipomatous hamartomas of the scalp and eyes are the hallmarks of this disorder.
  • Associated findings are extremely variable, ranging from minor abnormalities to severe, debilitating disease.
  • We report two unrelated Brazilian patients with encephalocraniocutaneous lipomatosis, one presenting with the full-blown spectrum of cutaneous, ocular, and central nervous system manifestations, and the other with minor extracutaneous manifestations after a 5-year follow-up period.
  • [MeSH-major] Abnormalities, Multiple / diagnosis. Craniofacial Abnormalities / diagnosis. Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis
  • [MeSH-minor] Alopecia / diagnosis. Biopsy, Needle. Brazil. Child. Child, Preschool. Eye Abnormalities / diagnosis. Female. Follow-Up Studies. Humans. Immunohistochemistry. Magnetic Resonance Imaging. Rare Diseases


47. Vinson EN, Dodd LG, Merian M, Martinez S: Synovial lipomatosis arborescens of the peroneal tendon sheath. Skeletal Radiol; 2008 Oct;37(10):947-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Synovial lipomatosis arborescens of the peroneal tendon sheath.
  • We advocate the term "synovial lipomatosis arborescens" for this process and present what is, to our knowledge, the first reported case of this disorder isolated to the peroneal tendon sheath, with imaging, intraoperative, and histological correlation.
  • [MeSH-major] Joint Diseases / diagnosis. Knee Joint / pathology. Lipomatosis / diagnosis. Synovial Membrane / pathology. Tendons / pathology

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  • [Cites] AJR Am J Roentgenol. 1996 Nov;167(5):1229-32 [8911186.001]
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  • (PMID = 18682928.001).
  • [ISSN] 0364-2348
  • [Journal-full-title] Skeletal radiology
  • [ISO-abbreviation] Skeletal Radiol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


48. Zeitler H, Ulrich-Merzenich G, Richter DF, Vetter H, Walger P: Multiple benign symmetric lipomatosis--a differential diagnosis of obesity. Is there a rationale for fibrate treatment? Obes Surg; 2008 Oct;18(10):1354-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple benign symmetric lipomatosis--a differential diagnosis of obesity. Is there a rationale for fibrate treatment?
  • Multiple benign symmetric lipomatosis (MSL) is characterized by a rapid progression of multiple, symmetric nonencapsulated fat masses in the face, neck, and extremities.
  • Multiple lipectomies were performed, but disease progressed.
  • Disease progression discontinued and circumferences of abdominal adipose tissue reduced.
  • [MeSH-major] Fenofibrate / therapeutic use. Hypolipidemic Agents / therapeutic use. Lipomatosis, Multiple Symmetrical / diagnosis. Lipomatosis, Multiple Symmetrical / drug therapy. Obesity / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Humans. Male. Middle Aged

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  • [Cites] Chirurg. 1997 Mar;68(3):276-9 [9198573.001]
  • [Cites] Clin Endocrinol (Oxf). 1987 Nov;27(5):601-6 [2897261.001]
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  • [Cites] Biochem Biophys Res Commun. 2005 Oct 14;336(1):76-83 [16125138.001]
  • [Cites] J Pathol. 2002 Nov;198(3):378-87 [12375271.001]
  • [Cites] Int J Dermatol. 2005 Mar;44(3):236-7 [15807734.001]
  • [Cites] Brain. 1988 Oct;111 ( Pt 5):1157-71 [3179687.001]
  • (PMID = 18528737.001).
  • [ISSN] 0960-8923
  • [Journal-full-title] Obesity surgery
  • [ISO-abbreviation] Obes Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Hypolipidemic Agents; U202363UOS / Fenofibrate
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49. Zielińska-Kaźmierska B, Grodecka J, Jabłońska-Polakowska L, Arkuszewski P: Mandibular osteoma in the encephalocraniocutaneous lipomatosis. J Craniomaxillofac Surg; 2005 Aug;33(4):286-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mandibular osteoma in the encephalocraniocutaneous lipomatosis.
  • INTRODUCTION: Encephalocraniocutaneous lipomatosis is a rare congenital disorder characterized by an abnormal development of adipose tissue, and is of unknown pathogenesis.
  • Catherine Haberland and Maurice Perou first diagnosed this disorder in 1970.
  • To our knowledge, approximately 25 patients have been reported with this diagnosis but so far, only 1 patient has been reported in Poland by Roszkowski and Dabrowski in 1997.
  • CONCLUSION: Encephalocraniocutaneous lipomatosis is a very rare syndrome.
  • Only a few authors described jaw tumours and no information was found on such big osteomas to this syndrome.
  • [MeSH-major] Craniotomy. Lipomatosis / complications. Mandibular Neoplasms / surgery. Osteoma / surgery
  • [MeSH-minor] Adult. Bone Transplantation. Facial Asymmetry / surgery. Female. Humans. Syndrome

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  • (PMID = 15975807.001).
  • [ISSN] 1010-5182
  • [Journal-full-title] Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
  • [ISO-abbreviation] J Craniomaxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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50. Heike Z, Gudrun UM, Frank RD, Vetter H, Walger P: Multiple benign symmetric lipomatosis--a differential diagnosis of obesity: is there a rationale for fibrate treatment? Obes Surg; 2008 Feb;18(2):240-2
MedlinePlus Health Information. consumer health - Obesity.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple benign symmetric lipomatosis--a differential diagnosis of obesity: is there a rationale for fibrate treatment?
  • Multiple benign symmetric lipomatosis (MSL) is characterized by a rapid progression of multiple, symmetric nonencapsulated fat masses in face, neck, and extremities.
  • Multiple lipectomies were performed but disease progressed.
  • Disease progression discontinued, and circumferences of abdominal adipose tissue reduced.
  • [MeSH-major] Clofibric Acid / therapeutic use. Lipomatosis, Multiple Symmetrical / diagnosis. Obesity / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Humans. Male. Middle Aged. Remission Induction

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  • [Cites] Chirurg. 1997 Mar;68(3):276-9 [9198573.001]
  • [Cites] Clin Endocrinol (Oxf). 1987 Nov;27(5):601-6 [2897261.001]
  • [Cites] Int J Obes Relat Metab Disord. 2002 Feb;26(2):253-61 [11850759.001]
  • [Cites] Biochem Biophys Res Commun. 2005 Oct 14;336(1):76-83 [16125138.001]
  • [Cites] J Pathol. 2002 Nov;198(3):378-87 [12375271.001]
  • [Cites] Int J Dermatol. 2005 Mar;44(3):236-7 [15807734.001]
  • [Cites] Brain. 1988 Oct;111 ( Pt 5):1157-71 [3179687.001]
  • (PMID = 18175197.001).
  • [ISSN] 0960-8923
  • [Journal-full-title] Obesity surgery
  • [ISO-abbreviation] Obes Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 53PF01Q249 / Clofibric Acid
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51. Shah JA, Flynn P, Choudhari KA: Idiopathic spinal epidural lipomatosis. Br J Neurosurg; 2005 Jun;19(3):265-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Idiopathic spinal epidural lipomatosis.
  • We report a rare case of paraparesis caused by thoracic spinal epidural lipomatosis in a female patient who did not have any recognized predisposing factor for this condition.
  • [MeSH-major] Lipomatosis / pathology. Spinal Cord Diseases / pathology

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  • (PMID = 16455531.001).
  • [ISSN] 0268-8697
  • [Journal-full-title] British journal of neurosurgery
  • [ISO-abbreviation] Br J Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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52. Reed SD, Evans DE: Necrotizing Infiltrative Lipomatosis in a Miniature Zebu Bull (Bos primigenius indicus). Vet Med Int; 2010;2010:810496
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Necrotizing Infiltrative Lipomatosis in a Miniature Zebu Bull (Bos primigenius indicus).
  • Lipomatosis is described in a miniature Zebu, Bos primigenius indicus, bull that died of perianesthetic complications.
  • This is the first pathologic description of lipomatosis that we are aware of in this species and breed of cattle.
  • Infiltration of multiple visceral organs is described and depicted along with comparison to previously published cases of lipomatosis in other breeds of cattle.

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  • (PMID = 20445793.001).
  • [ISSN] 2042-0048
  • [Journal-full-title] Veterinary medicine international
  • [ISO-abbreviation] Vet Med Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Egypt
  • [Other-IDs] NLM/ PMC2859684
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53. Scorza A, De Vito F, Fabiani O, Ranieri FM, Trappolini M: [Lipomatosis of interatrial septum and supraventricular arrhythmias]. Recenti Prog Med; 2007 Nov;98(11):565-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Lipomatosis of interatrial septum and supraventricular arrhythmias].
  • Lipomatosis of interatrial septum is a rare benign disorder characterized by fat accumulation into interatrial septum.
  • For this reason, it should be considered in differential diagnosis of other cardiac masses.
  • We report the typical case of lipomatosis of interatrial septum and atrial flutter.
  • [MeSH-major] Atrial Flutter / diagnosis. Atrial Flutter / etiology. Atrial Septum / pathology. Lipomatosis / complications. Lipomatosis / diagnosis
  • [MeSH-minor] Aged. Diagnosis, Differential. Echocardiography. Electrocardiography. Female. Humans. Magnetic Resonance Imaging

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  • (PMID = 18044406.001).
  • [ISSN] 0034-1193
  • [Journal-full-title] Recenti progressi in medicina
  • [ISO-abbreviation] Recenti Prog Med
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Italy
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54. Izadyar S, Kwan JY, Harati Y: Myeloneuropathic presentation of spinal epidural lipomatosis. J Clin Neuromuscul Dis; 2006 Mar;7(3):133-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Myeloneuropathic presentation of spinal epidural lipomatosis.
  • Spinal epidural lipomatosis (SEL) is accumulation of unencapsulated fat tissue within the epidural space of the spinal canal.
  • She was initially diagnosed with diabetic neuropathy; however, the presence of myelopathic signs led to further investigation and diagnosis of SEL.

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  • (PMID = 19078799.001).
  • [ISSN] 1537-1611
  • [Journal-full-title] Journal of clinical neuromuscular disease
  • [ISO-abbreviation] J Clin Neuromuscul Dis
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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55. Ardinger HH, Horii KA, Begleiter ML: Expanding the phenotype of oculoectodermal syndrome: possible relationship to encephalocraniocutaneous lipomatosis. Am J Med Genet A; 2007 Dec 15;143A(24):2959-62
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expanding the phenotype of oculoectodermal syndrome: possible relationship to encephalocraniocutaneous lipomatosis.
  • Oculoectodermal syndrome (OES) is characterized by epibulbar dermoids, aplasia cutis congenita, and other abnormalities.
  • Here, we report 2 new cases, review 13 previous cases, and propose that OES may be a mild variant of encephalocraniocutaneous lipomatosis (ECCL), differing primarily in its lack of intracranial pathology.
  • [MeSH-major] Abnormalities, Multiple / diagnosis. Eye Abnormalities / diagnosis. Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis. Skin Abnormalities / diagnosis
  • [MeSH-minor] Alopecia / diagnosis. Brain / abnormalities. Child. Child, Preschool. Diagnosis, Differential. Facies. Female. Hamartoma / diagnosis. Humans. Infant. Infant, Newborn. Male. Phenotype. Syndrome

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  • [Copyright] (c) 2007 Wiley-Liss, Inc.
  • (PMID = 17963257.001).
  • [ISSN] 1552-4833
  • [Journal-full-title] American journal of medical genetics. Part A
  • [ISO-abbreviation] Am. J. Med. Genet. A
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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56. Sanal HT, Kocaoğlu M, Yildirim D, Ors F: Multiple cardiac lipomas and pericardial lipomatosis: multidedector-row computer tomography findings. Int J Cardiovasc Imaging; 2007 Oct;23(5):655-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple cardiac lipomas and pericardial lipomatosis: multidedector-row computer tomography findings.
  • Here we reported the multidedector-row computer tomography (MDCT) findings of a nontuberosclerosis case with multiple cardiac lipomas along with pericardial lipomatosis, who presented with symptoms of left heart failure after a hysterectomy surgery but otherwise healthy before that operation.
  • [MeSH-major] Heart Failure / diagnostic imaging. Heart Neoplasms / diagnostic imaging. Incidental Findings. Lipoma / diagnostic imaging. Lipomatosis / diagnostic imaging. Neoplasms, Multiple Primary / diagnostic imaging. Pericardium / diagnostic imaging. Tomography, X-Ray Computed

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  • [Cites] J Comput Assist Tomogr. 2004 Nov-Dec;28(6):852-6 [15538164.001]
  • [Cites] AJR Am J Roentgenol. 2001 Apr;176(4):1066-8 [11264112.001]
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  • [Cites] Australas Radiol. 2000 Aug;44(3):321-4 [10974728.001]
  • (PMID = 17061026.001).
  • [ISSN] 1569-5794
  • [Journal-full-title] The international journal of cardiovascular imaging
  • [ISO-abbreviation] Int J Cardiovasc Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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57. Liu X, Wilcox CM, Nodit L, Lazenby AJ: Multiple gastrointestinal stromal tumors and lipomatosis. Arch Pathol Lab Med; 2008 Nov;132(11):1825-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple gastrointestinal stromal tumors and lipomatosis.
  • Although both multicentric gastrointestinal stromal tumor and gastrointestinal lipomatosis have been reported in association with a few genetic syndromes, there has been no report, to our knowledge, of their coexistence.
  • We feel that the coexistence of multiple lesions of these 2 rare diseases in this relatively young patient may represent a novel syndrome.
  • [MeSH-major] Duodenal Neoplasms / diagnosis. Gastrointestinal Stromal Tumors / diagnosis. Lipoma / diagnosis
  • [MeSH-minor] Adult. Humans. Male. Proto-Oncogene Proteins c-kit / metabolism

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  • (PMID = 18976023.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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58. Valladares MJ, Blanco MJ, Lopez-Lopez F, Gonzalez F: Bilateral ocular involvement in encephalocraniocutaneous lipomatosis. Eur J Paediatr Neurol; 2007 Mar;11(2):108-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Bilateral ocular involvement in encephalocraniocutaneous lipomatosis.
  • We report a case of encephalocraniocutaneous lipomatosis (ECCL), a rare congenital neurocutaneous syndrome, with cutaneous, ocular and neurologic malformations.
  • [MeSH-major] Eye Diseases / etiology. Functional Laterality. Lipomatosis / complications. Neurocutaneous Syndromes / complications

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  • (PMID = 17258481.001).
  • [ISSN] 1090-3798
  • [Journal-full-title] European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
  • [ISO-abbreviation] Eur. J. Paediatr. Neurol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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59. Pandzić Jaksić V, Bozkov V: From ancient enigmas to novel paradigms: a depiction of multiple symmetric lipomatosis. Coll Antropol; 2008 Jun;32(2):637-40

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] From ancient enigmas to novel paradigms: a depiction of multiple symmetric lipomatosis.
  • A rare case of multiple symmetric lipomatosis type 2 in a female patient was presented.
  • New possible iconographic representations of multiple symmetric lipomatosis were considered and some metabolic aspects of this disease were reviewed.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis

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  • (PMID = 18756923.001).
  • [ISSN] 0350-6134
  • [Journal-full-title] Collegium antropologicum
  • [ISO-abbreviation] Coll Antropol
  • [Language] eng
  • [Publication-type] Historical Article; Journal Article
  • [Publication-country] Croatia
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60. Miglani U, Sinha T, Gupta SK, Doddamani D, Sethi GS, Talwar R, Agrawal S, Chandra M, Rana YP, Harkar S: Rare etiology of obstructive uropathy: pelvic lipomatosis. Urol Int; 2010;84(2):239-41
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rare etiology of obstructive uropathy: pelvic lipomatosis.
  • We present a case of a 32-year-old hypertensive and obese male who had bilateral obstructive uropathy, and who was diagnosed as having pelvic lipomatosis on the basis of clinicoradiological findings.
  • [MeSH-major] Lipomatosis / diagnosis. Urologic Diseases / diagnosis. Urologic Diseases / etiology

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  • [Copyright] Copyright (c) 2010 S. Karger AG, Basel.
  • (PMID = 20215833.001).
  • [ISSN] 1423-0399
  • [Journal-full-title] Urologia internationalis
  • [ISO-abbreviation] Urol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  • [Chemical-registry-number] AYI8EX34EU / Creatinine
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61. Alkan O, Yildirim T, Seyhan T, Erbay G, Erol I: Congenital infiltrating lipomatosis of the face with hemimegalencephaly. Neuropediatrics; 2009 Jun;40(3):141-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital infiltrating lipomatosis of the face with hemimegalencephaly.
  • Congenital infiltrating lipomatosis of the face (CILF) is a rare disorder, causing unilateral facial asymmetry characterized by enlargement of the cheek or chin.
  • [MeSH-major] Facial Asymmetry / complications. Facial Asymmetry / congenital. Facial Neoplasms / complications. Facial Neoplasms / congenital. Lipomatosis / complications. Lipomatosis / congenital. Malformations of Cortical Development / complications

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  • (PMID = 20020401.001).
  • [ISSN] 1439-1899
  • [Journal-full-title] Neuropediatrics
  • [ISO-abbreviation] Neuropediatrics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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62. Rajput D, Srivastava AK, Kumar R: Spinal epidural lipomatosis: An unusual cause of relapsing and remitting paraparesis. J Pediatr Neurosci; 2010 Jul;5(2):150-2

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spinal epidural lipomatosis: An unusual cause of relapsing and remitting paraparesis.
  • Epidural lipomatosis is a rare entity to cause spinal cord compression and neurological deficits.
  • This is usually associated with excess of steroids in the body either because of endogenous source as in Cushings disease or exogenous intake as in some diseases like systemic lupus erythematosus, in some endocrinopathies or in morbid obesity.
  • Such idiopathic cases of spinal epidural lipomatosis have also been reported.
  • Here, we report a case of idiopathic spinal epidural lipomatosis with relapsing and remitting paraparesis which is quite unusual.

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  • [Cites] Eur Spine J. 2006 Jan;15(1):105-8 [16007467.001]
  • [Cites] Spine (Phila Pa 1976). 1991 Dec;16(12):1365-71 [1771466.001]
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  • [Cites] Spinal Cord. 2008 Mar;46(3):243-4 [17607308.001]
  • (PMID = 21559166.001).
  • [ISSN] 1998-3948
  • [Journal-full-title] Journal of pediatric neurosciences
  • [ISO-abbreviation] J Pediatr Neurosci
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3087997
  • [Keywords] NOTNLM ; Idiopathic cord compression / myelopathy / paraparesis / spinal epidural lipomatosis
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63. Leruth E, Coppens L, Andrianne R, Bonnet P, Waltregny D, de Leval J: [Pelvic lipomatosis associated with glandular cystitis. Report of two cases]. Prog Urol; 2005 Feb;15(1):81-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Pelvic lipomatosis associated with glandular cystitis. Report of two cases].
  • [Transliterated title] Lipomatose pelvienne associée à une cystite glandulaire: rapport de deux cas.
  • The authors report two cases of pelvic lipomatosis associated with glandular cystitis.
  • This is a rare disease with variable and nonspecific clinical features.
  • Complementary investigations useful for the diagnosis of pelvic lipomatosis are CT and especially MRI, intravenous urography and biopsies.
  • [MeSH-major] Cystitis / complications. Lipomatosis / etiology

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  • (PMID = 15822400.001).
  • [ISSN] 1166-7087
  • [Journal-full-title] Progrès en urologie : journal de l'Association française d'urologie et de la Société française d'urologie
  • [ISO-abbreviation] Prog. Urol.
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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64. Laouad I, Büchler M, Weestel PF, Lebranchu Y, Legendre C, Choukroun G, Thervet E: Replacement kidney lipomatosis after renal transplantation. Transplantation; 2005 Feb 27;79(4):496-8
MedlinePlus Health Information. consumer health - Kidney Transplantation.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Replacement kidney lipomatosis after renal transplantation.
  • Renal sinus lipomatosis consists of abnormal fatty proliferation of the renal sinus, hilus, and perirenal spaces.
  • We describe three cases of replacement kidney lipomatosis that occurred after cadaveric renal transplantation and discuss the possible differential diagnosis of this condition.
  • [MeSH-major] Kidney Diseases / etiology. Kidney Transplantation / adverse effects. Lipomatosis / etiology
  • [MeSH-minor] Adult. Aged. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Pyelonephritis, Xanthogranulomatous / pathology

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  • (PMID = 15729179.001).
  • [ISSN] 0041-1337
  • [Journal-full-title] Transplantation
  • [ISO-abbreviation] Transplantation
  • [Language] eng
  • [Publication-type] Case Reports
  • [Publication-country] United States
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65. Dominici F, Ginanneschi F, Spidalieri R, Rossi A: Multiple arm lipomatosis and posterior interosseus nerve palsy. Electromyogr Clin Neurophysiol; 2008 Nov-Dec;48(8):373-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple arm lipomatosis and posterior interosseus nerve palsy.
  • BACKGROUND: Lipomas are common benign soft tissue tumours which tend to be indolent and risk free.
  • METHODS (CASE DESCRIPTION): We present two patients with multiple lipomatosis of the arms and PIN paralysis, with a brief review of the cases reported in literature.
  • [MeSH-major] Electromyography. Lipomatosis / complications. Nerve Compression Syndromes / diagnosis. Nerve Compression Syndromes / etiology. Radial Neuropathy / diagnosis. Radial Neuropathy / etiology

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  • (PMID = 19097478.001).
  • [ISSN] 0301-150X
  • [Journal-full-title] Electromyography and clinical neurophysiology
  • [ISO-abbreviation] Electromyogr Clin Neurophysiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
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66. Chang SD, Coakley FV, Goldstein RB: Case report: Renal replacement lipomatosis associated with renal transplantation. Br J Radiol; 2005 Jan;78(925):60-1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Case report: Renal replacement lipomatosis associated with renal transplantation.
  • We report a case of extensive renal replacement lipomatosis demonstrated by ultrasound (US) and computed tomography (CT) in a 57-year-old woman with a history of two cadaveric renal transplants.
  • The second renal transplant is functioning normally and the renal replacement lipomatosis did not cause mass effect on either of the renal transplants.
  • [MeSH-major] Kidney Neoplasms / etiology. Kidney Transplantation / adverse effects. Lipomatosis / etiology


67. Takayama S, Sukekawa H, Arimoto T, Ikeno E, Komatu T, Rikimaru H, Hakamatsuka T, Takahashi T, Sugawara M: Lipomatous hypertrophy of the interatrial septum with cutaneous lipomatosis. Circ J; 2007 Jun;71(6):986-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Lipomatous hypertrophy of the interatrial septum with cutaneous lipomatosis.
  • In order to discriminate the myocardial lesion from myxoma and other benign conditions and malignant tumors, percutaneous transvenous biopsy was performed.
  • The LHIS is itself a rare condition, and its development in patients having multiple ponderous lipomas, or lipomatosis, could not be found in a previous report.
  • This may be the first published case of LHIS, which likely represents cardiac involvement of lipomatosis.
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Lipomatosis / pathology. Myxoma / pathology

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  • (PMID = 17527001.001).
  • [ISSN] 1346-9843
  • [Journal-full-title] Circulation journal : official journal of the Japanese Circulation Society
  • [ISO-abbreviation] Circ. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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68. Hudolin T, Kastelan Z, Goluza E, Basić-Jukić N, Sosić H: Pelvic and retroperitoneal lipomatosis: case report. Acta Clin Croat; 2010 Dec;49(4):465-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pelvic and retroperitoneal lipomatosis: case report.
  • A rare case of pelvic and retroperitoneal lipomatosis lasting for more then three decades is presented.
  • Although the disease is benign, it is usually progressive and may lead to renal insufficiency.
  • The clinical features, intravenous urography, computed tomography and magnetic resonance images, differential diagnosis and therapeutic aspects of this rare disease are presented.
  • [MeSH-major] Lipomatosis / diagnosis. Pelvis. Retroperitoneal Space

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  • (PMID = 21830459.001).
  • [ISSN] 0353-9466
  • [Journal-full-title] Acta clinica Croatica
  • [ISO-abbreviation] Acta Clin Croat
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Croatia
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69. Kim HK, Lee JY, Kim WS, Bae TH: Atypical diffuse lipomatosis with multifocal abdominal involvement: a case report. J Plast Reconstr Aesthet Surg; 2010 Oct;63(10):e742-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical diffuse lipomatosis with multifocal abdominal involvement: a case report.
  • We present the case of an 8-year-old child with diffuse lipomatosis simultaneously involving the intra-peritoneum, retro-peritoneum and abdominal wall.
  • To the best of our knowledge, this is the first case of diffuse lipomatosis with simultaneous multi-focal involvement of the entire abdomen.
  • [MeSH-major] Abdominal Wall / surgery. Lipomatosis / surgery. Peritoneum / surgery

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  • [Copyright] Copyright 2010 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20541989.001).
  • [ISSN] 1878-0539
  • [Journal-full-title] Journal of plastic, reconstructive & aesthetic surgery : JPRAS
  • [ISO-abbreviation] J Plast Reconstr Aesthet Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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70. Calisir C, Can C, Kebapci M: Renal replacement lipomatosis: multidetector-row computed tomography findings in one case. Acta Radiol; 2007 Mar;48(2):242-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Renal replacement lipomatosis: multidetector-row computed tomography findings in one case.
  • Replacement lipomatosis of the kidney is the result of severe atrophy of the renal parenchyma often caused by chronic calculus disease with secondary marked benign proliferation of fibrofatty tissue replacing atrophied renal parenchyma.
  • We report multidedector CT (MDCT) findings of replacement lipomatosis in a 50-year-old woman.
  • We think that it accurately provides a complete one-step diagnostic workup and appropriate pre-surgical planning for patients for whom there is a suspicion of replacement lipomatosis.
  • [MeSH-major] Kidney Diseases / radiography. Lipomatosis / radiography. Tomography, X-Ray Computed / methods

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  • (PMID = 17354149.001).
  • [ISSN] 0284-1851
  • [Journal-full-title] Acta radiologica (Stockholm, Sweden : 1987)
  • [ISO-abbreviation] Acta Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Sweden
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71. Sabharwal S, Mahmood F: Thoracic spinal epidural lipomatosis associated with adolescent scoliosis. J Spinal Disord Tech; 2006 May;19(3):217-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Thoracic spinal epidural lipomatosis associated with adolescent scoliosis.
  • Although a variety of neural axis abnormalities in association with idiopathic scoliosis have been reported, there are no documented cases of spinal epidural lipomatosis (SEL) in a child with scoliosis.
  • [MeSH-major] Lipomatosis / complications. Lipomatosis / diagnosis. Scoliosis / complications. Scoliosis / diagnosis. Spinal Diseases / complications. Spinal Diseases / diagnosis. Thoracic Vertebrae / surgery

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  • (PMID = 16770223.001).
  • [ISSN] 1536-0652
  • [Journal-full-title] Journal of spinal disorders & techniques
  • [ISO-abbreviation] J Spinal Disord Tech
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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72. Sairyo K, Sakai T, Higashino K, Hirao B, Katoh S, Yasui N: Minimally invasive excision of lumbar epidural lipomatosis using a spinal endoscope. Minim Invasive Neurosurg; 2008 Feb;51(1):43-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Minimally invasive excision of lumbar epidural lipomatosis using a spinal endoscope.
  • In this report, we describe the case of a patient with a long-term radiculopathy due to epidural lipomatosis at the L3-4 intervertebral disc level.
  • We would like to state that epidural lipomatosis is a good candidate for minimally invasive endoscopic surgery because of its anatomic location.
  • [MeSH-major] Endoscopy / methods. Epidural Space / surgery. Lipomatosis / surgery. Lumbar Vertebrae / surgery. Polyradiculopathy / surgery

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  • (PMID = 18306131.001).
  • [ISSN] 0946-7211
  • [Journal-full-title] Minimally invasive neurosurgery : MIN
  • [ISO-abbreviation] Minim Invasive Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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73. Min WK, Oh CW, Jeon IH, Kim SY, Park BC: Decompression of idiopathic symptomatic epidural lipomatosis of the lumbar spine. Joint Bone Spine; 2007 Oct;74(5):488-90
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Decompression of idiopathic symptomatic epidural lipomatosis of the lumbar spine.
  • Epidural lipomatosis has been implicated as a cause or contributor of symptomatic lumbar spinal stenosis.
  • Symptomatic spinal epidural lipomatosis (SEL) of the lumbar spine is a rare disease, often associated with steroid overload.
  • Idiopathic lipomatosis is even much less frequent.
  • Diagnosis is best based on MRI.
  • Obesity, endocrinopathic disease, and chronic steroid therapy were excluded.
  • [MeSH-major] Decompression / methods. Lipomatosis / diagnosis. Spinal Diseases / diagnosis

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  • (PMID = 17681857.001).
  • [ISSN] 1778-7254
  • [Journal-full-title] Joint, bone, spine : revue du rhumatisme
  • [ISO-abbreviation] Joint Bone Spine
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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74. Zahariev ZI, Peycheva MV, Dobrev HP: A case of encephalocraniocutaneous lipomatosis syndrome with epilepsy (Haberland syndrome). Folia Med (Plovdiv); 2009 Oct-Dec;51(4):46-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of encephalocraniocutaneous lipomatosis syndrome with epilepsy (Haberland syndrome).
  • Encephalocraniocutaneous lipomatosis is a rare congenital neurocutaneous syndrome characterized by scalp, facial, and ocular lesions and multiple intracranial malformations.
  • [MeSH-major] Epilepsy / diagnosis. Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis. Skin / pathology
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging

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  • (PMID = 20232658.001).
  • [ISSN] 0204-8043
  • [Journal-full-title] Folia medica
  • [ISO-abbreviation] Folia Med (Plovdiv)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Bulgaria
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75. Burkhardt N, Hamann GF: [Extradural lipomatosis after long-term treatment with steroids]. Nervenarzt; 2006 Dec;77(12):1477-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Extradural lipomatosis after long-term treatment with steroids].
  • [Transliterated title] Extradurale Lipomatose nach langjähriger Steroidbehandlung.
  • Epidural lipomatosis is a rare but severe complication of long-term corticoid treatment.
  • [MeSH-major] Anti-Inflammatory Agents / adverse effects. Giant Cell Arteritis / drug therapy. Lipomatosis / chemically induced. Prednisolone / adverse effects. Spinal Cord Compression / diagnosis. Spinal Diseases / chemically induced. Thoracic Vertebrae
  • [MeSH-minor] Diagnosis, Differential. Dose-Response Relationship, Drug. Epidural Space. Female. Humans. Laminectomy. Long-Term Care. Magnetic Resonance Imaging. Middle Aged. Neurologic Examination

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  • [Cites] Neurosurgery. 1993 Sep;33(3):374-8 [8413866.001]
  • [Cites] N Engl J Med. 1983 Feb 10;308(6):316-9 [6337324.001]
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  • (PMID = 17093956.001).
  • [ISSN] 0028-2804
  • [Journal-full-title] Der Nervenarzt
  • [ISO-abbreviation] Nervenarzt
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 9PHQ9Y1OLM / Prednisolone
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76. Choh NA, Jehangir M, Choh SA: Renal replacement lipomatosis: A rare type of renal pseudotumor. Indian J Nephrol; 2010 Apr;20(2):92-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Renal replacement lipomatosis: A rare type of renal pseudotumor.
  • Replacement lipomatosis of the kidney is the end result of severe atrophy of renal parenchyma with secondary marked proliferation of renal sinus and perirenal fatty tissue.
  • Although ultrasonography may suggest the diagnosis, CT demonstrated the distinctive features most accurately.
  • We report a case of renal replacement lipomatosis with coexistent xanthogranulomatous pyelonephritis and multiple perinephric and parietal wall collections.

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  • (PMID = 20835324.001).
  • [ISSN] 1998-3662
  • [Journal-full-title] Indian journal of nephrology
  • [ISO-abbreviation] Indian J Nephrol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC2931141
  • [Keywords] NOTNLM ; Pseudotumor / kidney / lipomatosis
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77. Bansal M, Changulani M, Shukla R, Sampath J: Synovial lipomatosis of the knee in an adolescent girl. Orthopedics; 2008 Feb;31(2):185
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  • [Title] Synovial lipomatosis of the knee in an adolescent girl.
  • Synovial lipomatosis is an uncommon intraarticular lesion rarely affecting the pediatric age group.
  • It should be considered in the differential diagnosis of refractory chronic joint effusion and synovial swelling around the knee joint.
  • MRI is helpful in the diagnosis of this pathology.
  • She was found to have Synovial Lipomatosis of the knee joint, which was excised arthroscopically.
  • Synovial lipomatosis is a rare diagnosis in childhood.
  • It should be considered in the differential diagnosis of refractory chronic joint effusion and synovial swelling around the knee joint.
  • Magnetic resonance imaging may be helpful in the diagnosis of these cases, but confirmation can only be obtained through histology.
  • [MeSH-major] Cartilage Diseases / diagnosis. Cartilage Diseases / surgery. Joint Diseases / diagnosis. Joint Diseases / surgery. Knee Joint / surgery. Lipomatosis / diagnosis. Lipomatosis / surgery. Synovial Membrane / surgery

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  • (PMID = 19292183.001).
  • [ISSN] 0147-7447
  • [Journal-full-title] Orthopedics
  • [ISO-abbreviation] Orthopedics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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78. Kamal D, Breton P, Bouletreau P: Congenital infiltrating lipomatosis of the face: report of three cases and review of the literature. J Craniomaxillofac Surg; 2010 Dec;38(8):610-4

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  • [Title] Congenital infiltrating lipomatosis of the face: report of three cases and review of the literature.
  • OBJECTIVES: Three new cases of hemifacial hypertrophy caused by congenital infiltrating lipomatosis of the face are reported.
  • The literature on infiltrating lipomatosis of the face is reviewed with an emphasis on accompanying anomalies and treatment strategies.
  • REPORT OF CASES: In this study, the clinical features, radiographic findings, histopathology, and postoperative results were analyzed in three patients with facial infiltrating lipomatosis.
  • DISCUSSION: Described first by Slavin and colleagues in 1989, Facial infiltrating lipomatosis is a rare congenital disorder in which mature lipocytes invade adjacent tissue.
  • [MeSH-major] Facial Asymmetry / congenital. Facial Neoplasms / congenital. Lipomatosis / congenital

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  • [Copyright] Copyright © 2010 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20338773.001).
  • [ISSN] 1878-4119
  • [Journal-full-title] Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
  • [ISO-abbreviation] J Craniomaxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Scotland
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79. Al-Khawaja D, Seex K, Eslick GD: Spinal epidural lipomatosis--a brief review. J Clin Neurosci; 2008 Dec;15(12):1323-6
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  • [Title] Spinal epidural lipomatosis--a brief review.
  • Spinal epidural lipomatosis (SEL) is a rare disorder characterized by overgrowth of fat in the extradural space, causing compression of the neural elements.
  • One was 53-year-old man with progressive mid-thoracic and lower limb pain with associated weakness and neurogenic claudication due to thoracic epidural lipomatosis.
  • The second was a 68-year-old male with lumbar epidural lipomatosis.
  • An MRI revealed stenosis at L4-S1 and diffuse anterior lipomatosis.
  • [MeSH-major] Epidural Space / pathology. Lipomatosis / pathology. Spinal Cord Diseases / pathology

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  • (PMID = 18954986.001).
  • [ISSN] 0967-5868
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Scotland
  • [Number-of-references] 63
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80. Maruyama K, Okumura A, Negoro T, Watanabe K: Congenital infiltrating lipomatosis of the face with ipsilateral hemimegalencephaly, band heterotopia, and hypertrophy of brainstem and cerebellum. Neuropediatrics; 2010 Jun;41(3):147-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital infiltrating lipomatosis of the face with ipsilateral hemimegalencephaly, band heterotopia, and hypertrophy of brainstem and cerebellum.
  • The simultaneous appearance of congenital infiltrating lipomatosis of the face that causes facial hemihypertrophy and ipsilateral hemimegalencephaly is extremely rare.
  • Magnetic resonance imaging (MRI) results led to the diagnosis of infiltrating lipomatosis of the face; the diagnosis was confirmed on the basis of the results of pathological examinations.
  • He had no nevi or other skin abnormalities suggesting neurocutaneous syndrome.
  • [MeSH-major] Brain / abnormalities. Functional Laterality. Lipomatosis / complications. Malformations of Cortical Development / complications. Malformations of Cortical Development / pathology

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  • [Copyright] © Georg Thieme Verlag KG Stuttgart · New York.
  • (PMID = 20859836.001).
  • [ISSN] 1439-1899
  • [Journal-full-title] Neuropediatrics
  • [ISO-abbreviation] Neuropediatrics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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81. Möller J, Girschick HJ, Hahn G, Pessler F: [Steroid-induced spinal epidural lipomatosis in pediatric patients]. Z Rheumatol; 2010 Jul;69(5):447-9
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  • [Title] [Steroid-induced spinal epidural lipomatosis in pediatric patients].
  • [Transliterated title] Kortikosteroid-induzierte spinale epidurale Lipomatose bei pädiatrischen Patienten.
  • In all cases, MRI showed extensive spinal epidural lipomatosis, a rare but classic untoward effect of chronic glucocorticoid therapy.
  • Analysis of these three, as well as 11 other pediatric cases extracted from the international literature, revealed that spinal epidural lipomatosis manifests most commonly with back pain and within a mean of 1.3 years (range, 3 month-6.5 years) after initiation of therapy with corticosteroids.
  • [MeSH-major] Anti-Inflammatory Agents / adverse effects. Arthritis, Juvenile / drug therapy. Epidural Space. Lipomatosis / chemically induced. Lupus Erythematosus, Systemic / drug therapy. Methylprednisolone / adverse effects. Prednisolone / adverse effects. Sjogren's Syndrome / drug therapy. Spinal Cord Diseases / chemically induced
  • [MeSH-minor] Adolescent. Child. Drug Therapy, Combination. Female. Humans. Immunosuppressive Agents / adverse effects. Immunosuppressive Agents / therapeutic use. Lumbar Vertebrae / pathology. Spinal Cord Compression / chemically induced. Spinal Cord Compression / diagnosis. Thoracic Vertebrae / pathology

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  • [Cites] Arthritis Rheum. 1988 Mar;31(3):447-51 [3358807.001]
  • [Cites] Med J Aust. 1975 Feb 15;1(7):201-3 [1092979.001]
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  • (PMID = 20213089.001).
  • [ISSN] 1435-1250
  • [Journal-full-title] Zeitschrift fur Rheumatologie
  • [ISO-abbreviation] Z Rheumatol
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Immunosuppressive Agents; 9PHQ9Y1OLM / Prednisolone; X4W7ZR7023 / Methylprednisolone
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82. Gill JB: Fat suppression imaging in epidural lipomatosis: case report. J Surg Orthop Adv; 2007;16(3):144-7
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  • [Title] Fat suppression imaging in epidural lipomatosis: case report.
  • A case of epidural lipomatosis associated with steroid use in rheumatoid arthritis is presented to describe the role of fat suppression imaging as a diagnostic tool.
  • A fat suppression MRI was obtained, which confirmed the diagnosis of epidural lipomatosis.
  • An MRI scan is the imaging tool of choice to examine soft tissue lesions of the spine, and fat suppression imaging will provide additional information about any fatty soft tissue lesion, as in the case of epidural lipomatosis.
  • This imaging modality is particularly useful in those patients who are morbidly obese or taking exogenous corticosteroids, because these conditions can proliferate adipose tissue leading to epidural lipomatosis.
  • [MeSH-major] Adipose Tissue. Image Enhancement / methods. Lipomatosis / diagnosis. Magnetic Resonance Imaging / methods. Spinal Diseases / diagnosis. Thoracic Vertebrae / pathology

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  • (PMID = 17963658.001).
  • [ISSN] 1548-825X
  • [Journal-full-title] Journal of surgical orthopaedic advances
  • [ISO-abbreviation] J Surg Orthop Adv
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Glucocorticoids; VB0R961HZT / Prednisone
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83. Bergmann T, Hösl K, Hahn EG, Harsch IA: [Metabolical characteristics in patients with multiple symmetrical lipomatosis]. Dtsch Med Wochenschr; 2008 Nov;133(45):2323-7
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  • [Title] [Metabolical characteristics in patients with multiple symmetrical lipomatosis].
  • [Transliterated title] Metabolische Besonderheiten bei Patienten mit Multipler Symmetrischer Lipomatose.
  • BACKGROUND AND OBJECTIVE: Multiple symmetrical lipomatosis (MSL) is a rare cause of obesity.
  • The possible presence of an obstructive sleep apnoea syndrome was also looked for.
  • RESULTS: Five of the 15 patients fulfilled the International Diabetes Federation's criteria of a metabolic syndrome.
  • But the prevalence of the (cardio)metabolic syndrome is relatively high.
  • Thus an elevated risk of cardiovascular disease in these patients is likely.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / metabolism. Metabolic Syndrome X / complications. Parathyroid Hormone / blood

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  • (PMID = 18958827.001).
  • [ISSN] 1439-4413
  • [Journal-full-title] Deutsche medizinische Wochenschrift (1946)
  • [ISO-abbreviation] Dtsch. Med. Wochenschr.
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Parathyroid Hormone
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84. Durr ML, Agrawal N, Saunders JR, Ha PK: Laryngeal lipoma associated with diffuse lipomatosis: case report and literature review. Ear Nose Throat J; 2010 Jan;89(1):34-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laryngeal lipoma associated with diffuse lipomatosis: case report and literature review.
  • Lipomas are benign mesenchymal tumors that are often found in the head and neck.
  • We report a case of a laryngeal lipoma that was associated with diffuse systemic lipomatosis.
  • To the best of our knowledge, this is only the second case of laryngeal lipoma associated with lipomatosis to be reported in the English-language literature.
  • [MeSH-major] Laryngeal Neoplasms / epidemiology. Laryngeal Neoplasms / pathology. Lipoma / pathology. Lipomatosis / epidemiology

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  • (PMID = 20155698.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 10
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85. Dabrowska A, Tarnowska C, Jałowinski R, Stankiewicz J, Grzegorz M: [Multiple symmetric lipomatosis in the otolaryngology as diagnostic and therapeutic problem]. Otolaryngol Pol; 2005;59(5):717-22
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  • [Title] [Multiple symmetric lipomatosis in the otolaryngology as diagnostic and therapeutic problem].
  • Multiple symmetric lipomatosis (MSL) is a systemic disease connected with a degeneration of the adipose tissue.
  • Lipomatosis was initially described in 1846 by Brodie but the exact aetiopathogenesis is still unknown.
  • Depending on the anatomical location of the lipomatosis we can divided MSL into two types.
  • MATERIAL, METHODS AND THERAPY: We describe the findings in three patients with symmetric lipomatosis: two (n=2) with the first and one (n=1) with the second type of the disease.
  • Two patients received the pharmacological treatment (magnesium and the vitamin B6) and we observed marked regress of the disease.
  • Our observations indicate the efficiency of the magnesium and the vitamin B6 therapy in patients with multiple symmetric lipomatosis.
  • We want to underline that there are any research of the influence of the magnesium and the vitamin B6 on the course of this disease in the literature.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / diagnosis. Lipomatosis, Multiple Symmetrical / therapy
  • [MeSH-minor] Adipose Tissue / metabolism. Adult. Humans. Lipectomy. Magnesium / administration & dosage. Male. Middle Aged. Treatment Outcome. Vitamin B 6 / administration & dosage

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  • (PMID = 16471190.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
  • [Chemical-registry-number] 8059-24-3 / Vitamin B 6; I38ZP9992A / Magnesium
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86. Nardone R, Venturi A, Ladurner G, Golaszewski S, Psenner K, Tezzon F: Obturator mononeuropathy caused by lipomatosis of the nerve: a case report. Muscle Nerve; 2008 Aug;38(2):1046-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Obturator mononeuropathy caused by lipomatosis of the nerve: a case report.
  • Abdomino-pelvic computed tomography revealed a fusiform mass in the right perivesical space; magnetic resonance imaging (MRI) showed characteristic "coaxial-cable-like" appearance in cross-section and "spaghetti-like" appearance in longitudinal section, pathognomonic of lipomatosis of the nerve.
  • Nerve lipomatosis as the cause of obturator neuropathy has not been previously reported.
  • MRI provides definite and graphic proof of the diagnosis.
  • [MeSH-major] Lipomatosis / complications. Lipomatosis / pathology. Mononeuropathies / etiology. Nerve Tissue / pathology

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  • (PMID = 18508348.001).
  • [ISSN] 0148-639X
  • [Journal-full-title] Muscle & nerve
  • [ISO-abbreviation] Muscle Nerve
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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87. Pandzić Jaksić V, Stoos Veić T: Multiple symmetric lipomatosis type 2 in females--report of two cases. Acta Dermatovenerol Croat; 2008;16(1):31-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple symmetric lipomatosis type 2 in females--report of two cases.
  • Two patients with features of multiple symmetric lipomatosis type 2 are presented.
  • This particular disorder with a characteristic distribution of fat should be considered on differential diagnosis of obesity.
  • Patients with multiple symmetric lipomatosis should be treated by liposuction or surgery instead of being submitted to diets.
  • [MeSH-major] Lipomatosis, Multiple Symmetrical / pathology

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  • (PMID = 18358107.001).
  • [ISSN] 1847-6538
  • [Journal-full-title] Acta dermatovenerologica Croatica : ADC
  • [ISO-abbreviation] Acta Dermatovenerol Croat
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Croatia
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88. Suárez Moreno RM, Hernández Ramírez DA, Madrazo Navarro M, Salazar Lozano CR, Martínez Gen R: Multiple intestinal lipomatosis. Case report. Cir Cir; 2010 Mar-Apr;78(2):163-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple intestinal lipomatosis. Case report.
  • BACKGROUND: Intestinal lipomatosis is a rare disease with an incidence at autopsy ranging from 0.04 to 4.5%.
  • CONCLUSIONS: Benign tumors of the small bowel are relatively rare, with lipoma being the most common type.
  • With these typical radiographic findings, preoperative diagnosis is possible keeping in mind this rare disease.
  • [MeSH-major] Intestinal Diseases / diagnosis. Intestine, Small. Lipomatosis / diagnosis

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  • (PMID = 20478119.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] eng; spa
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Mexico
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89. Zuccoli G, Pipitone N, De Carli N, Vecchia L, Bartoletti SC: Acute spinal cord compression due to epidural lipomatosis complicated by an abscess: magnetic resonance and pathology findings. Eur Spine J; 2010 Jul;19 Suppl 2:S216-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Acute spinal cord compression due to epidural lipomatosis complicated by an abscess: magnetic resonance and pathology findings.
  • MR images of the thoracic spine were interpreted as being consistent with an abscess within an epidural lipomatosis compressing the spinal cord.
  • Laminectomy was performed, and a large amount of pus was drained from the epidural lipomatosis, from which Staphylococcus aureus was isolated.
  • This is the first reported case of an abscess involving an epidural lipomatosis.
  • [MeSH-major] Abscess / pathology. Lipomatosis / pathology. Spinal Cord Compression / pathology. Spinal Diseases / pathology. Staphylococcal Infections / pathology
  • [MeSH-minor] Acute Disease. Aged. Humans. Male. Treatment Outcome

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  • (PMID = 20372939.001).
  • [ISSN] 1432-0932
  • [Journal-full-title] European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
  • [ISO-abbreviation] Eur Spine J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Other-IDs] NLM/ PMC2899645
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90. Jamali M, Zouhair K, El Ouazzani T, Lakhdar H: [Precocious mediastinal lipomatosis: a rare complication of systemic corticosteroid therapy]. Ann Dermatol Venereol; 2006 Mar;133(3):257-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Precocious mediastinal lipomatosis: a rare complication of systemic corticosteroid therapy].
  • [Transliterated title] Lipomatose médiastinale précoce: une complication exceptionnelle de la corticothérapie generale.
  • BACKGROUND: Corticosteroid-induced lipomatosis results from hypertrophy within adipose tissue; the condition is frequently asymptomatic and its incidence is underestimated.
  • We report a case of mediastinal lipomatosis that is rare in terms of both site and presenting symptoms.
  • CASE REPORT: A 46-year-old woman with no disease history other than obesity with a weight of 90 kg had been treated since 2002 for mixed connective tissue disease (profound lupus and dermatomyositis).
  • The chest CT scan showed lipomatosis throughout the entire mediastinum with no associated chest abnormalities or pericardial effusion.
  • The chest scan performed two months later short stabilization of the patient's mediastinal lipomatosis.
  • DISCUSSION: The effects of long-term of glucocorticosteroid therapy are well-known, in particular Cushing's syndrome.
  • Lipomatosis has been described more recently and affects different axial regions.
  • [MeSH-major] Adrenal Cortex Hormones / adverse effects. Lipomatosis / chemically induced. Mediastinal Diseases / chemically induced
  • [MeSH-minor] Female. Humans. Middle Aged. Mixed Connective Tissue Disease / drug therapy

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  • (PMID = 16800178.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Adrenal Cortex Hormones
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91. Khallouk A, Tazi MF, Elfassi MJ, Farih MH: Chronic spontaneous nephrocutaneous fistula associated with renal replacement lipomatosis. Rev Urol; 2010;12(4):e190-2

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chronic spontaneous nephrocutaneous fistula associated with renal replacement lipomatosis.
  • Chronic spontaneous nephrocutaneous fistula is a rare renal disease.
  • Renal replacement lipomatosis (RRL) is the result of the atrophy and destruction of renal parenchyma with massive increases in the amount of fat in the sinus and perirenal space.
  • Indeed, urolithiasis is the most common cause of these diseases.

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  • [Cites] Eur Radiol. 2002 Apr;12(4):810-3 [11960231.001]
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  • (PMID = 21234262.001).
  • [ISSN] 2153-8182
  • [Journal-full-title] Reviews in urology
  • [ISO-abbreviation] Rev Urol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3020281
  • [Keywords] NOTNLM ; Nephrocutaneous fistula / Renal replacement lipomatosis / Renal tuberculosis
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92. Gönül M, Soylu S, Gül U, Aslan E, Unal T, Ergül G: Giant congenital melanocytic naevus associated with Dandy-Walker malformation, lipomatosis and hemihypertrophy of the leg. Clin Exp Dermatol; 2009 Jul;34(5):e106-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant congenital melanocytic naevus associated with Dandy-Walker malformation, lipomatosis and hemihypertrophy of the leg.
  • A few case reports relating to the coexistence of giant congenital melanocytic naevus, lipomatosis and hemihypertrophy have been published in the literature.
  • We report this very rare case of giant melanocytic naevus with lipomatosis, hemihypertrophy of the leg, and DWM.
  • [MeSH-major] Dandy-Walker Syndrome / diagnosis. Leg / pathology. Lipomatosis / diagnosis. Neurocutaneous Syndromes / diagnosis. Nevus, Pigmented / diagnosis
  • [MeSH-minor] Adult. Female. Humans. Hypertrophy / diagnosis. Magnetic Resonance Imaging

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  • (PMID = 19438567.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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93. Caux F, Plauchu H, Chibon F, Faivre L, Fain O, Vabres P, Bonnet F, Selma ZB, Laroche L, Gérard M, Longy M: Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity. Eur J Hum Genet; 2007 Jul;15(7):767-73
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity.
  • We describe two patients from distinct Cowden disease families with specific germline PTEN mutations whose disease differs from the usual appearance of Cowden disease.
  • Their phenotype associates classical manifestations of Cowden disease and congenital dysmorphisms including segmental overgrowth, arteriovenous and lymphatic vascular malformations, lipomatosis and linear epidermal nevus reminiscent of the diagnosis of Proteus syndrome.
  • Finally, we suggest using the term 'SOLAMEN syndrome' (Segmental Overgrowth, Lipomatosis, Arteriovenous Malformation and Epidermal Nevus) in these peculiar situations to help the difficult distinction between the phenotype of our patients and Proteus syndrome.
  • [MeSH-major] Abnormalities, Multiple / genetics. Hamartoma Syndrome, Multiple / genetics. PTEN Phosphohydrolase / genetics
  • [MeSH-minor] Adolescent. Adult. Arteriovenous Malformations / genetics. Arteriovenous Malformations / pathology. Child. Child, Preschool. Female. Germ-Line Mutation. Humans. Infant. Infant, Newborn. Lipomatosis / genetics. Middle Aged. Mutation, Missense. Nevus / genetics. Nevus / pathology. Pedigree. Syndrome


94. Wong BZ, Amrami KK, Wenger DE, Dyck PJ, Scheithauer BW, Spinner RJ: Lipomatosis of the sciatic nerve: typical and atypical MRI features. Skeletal Radiol; 2006 Mar;35(3):180-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Lipomatosis of the sciatic nerve: typical and atypical MRI features.
  • Lipomatosis of nerve, also known as fibrolipomatous hamartoma, is a rare condition of nerve, usually affecting the median nerve.
  • We describe two cases of lipomatosis of nerve involving the sciatic nerve, an extremely unusual location for this lesion, in patients with sciatic neuropathy.
  • [MeSH-major] Lipomatosis / diagnosis. Magnetic Resonance Imaging. Sciatic Nerve
  • [MeSH-minor] Adult. Aged. Diagnosis, Differential. Female. Humans. Male

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  • (PMID = 16283177.001).
  • [ISSN] 0364-2348
  • [Journal-full-title] Skeletal radiology
  • [ISO-abbreviation] Skeletal Radiol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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95. Gokhale NR, Mahajan PM, Belgaumkar VA, Pradhan SN, Uttarwar NS: Encephalocraniocutaneous lipomatosis: a rare neurocutaneous syndrome. Indian J Dermatol Venereol Leprol; 2007 Jan-Feb;73(1):40-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Encephalocraniocutaneous lipomatosis: a rare neurocutaneous syndrome.
  • Encephalocraniocutaneous lipomatosis is a congenital hamartomatous disorder with unique ocular, cutaneous and neurological features.
  • The constellation of these findings led us to a diagnosis of encephalocraniocutaneous lipomatosis.
  • [MeSH-major] Brain Diseases / pathology. Hamartoma / pathology. Lipomatosis / pathology. Neurocutaneous Syndromes / pathology. Skin Diseases / pathology
  • [MeSH-minor] Adolescent. Humans. Male. Rare Diseases / pathology

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  • (PMID = 17314447.001).
  • [ISSN] 0973-3922
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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96. Kadmon E, Paz R, Kusniec J, Strasberg B: Sick sinus syndrome in a patient with extensive cardiac lipomatosis (sinus node dysfunction in lipomatosis). Pacing Clin Electrophysiol; 2010 Apr;33(4):513-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sick sinus syndrome in a patient with extensive cardiac lipomatosis (sinus node dysfunction in lipomatosis).
  • We present a case of a 45-year-old man with an incidental and longstanding diagnosis of extensive mediastinal and cardiac lipomatosis.
  • There are many reports of cardiac lipomatosis in the literature, including reports of related ventricular arrhythmias, some of which are fatal. (PACE 2010; 513-515).
  • [MeSH-major] Bradycardia / therapy. Defibrillators, Implantable. Lipomatosis / complications. Sick Sinus Syndrome / therapy. Tachycardia, Ventricular / therapy

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  • (PMID = 19793369.001).
  • [ISSN] 1540-8159
  • [Journal-full-title] Pacing and clinical electrophysiology : PACE
  • [ISO-abbreviation] Pacing Clin Electrophysiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 8
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97. Fogel GR, Cunningham PY 3rd, Esses SI: Spinal epidural lipomatosis: case reports, literature review and meta-analysis. Spine J; 2005 Mar-Apr;5(2):202-11

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spinal epidural lipomatosis: case reports, literature review and meta-analysis.
  • BACKGROUND CONTEXT: Symptomatic spinal epidural lipomatosis (SEL), a rare cause of spinal cord compression, has most often been associated with exogenous steroid use.
  • PURPOSE: Identify four associations with SEL, correlate the associated groups with level of disease and compare treatment with outcome data in these groups.
  • With increased awareness of this condition and improved imaging techniques, further studies of this disease should be undertaken.
  • [MeSH-major] Lipomatosis / pathology. Spinal Cord Compression / pathology

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  • (PMID = 15795966.001).
  • [ISSN] 1529-9430
  • [Journal-full-title] The spine journal : official journal of the North American Spine Society
  • [ISO-abbreviation] Spine J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Meta-Analysis
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Glucocorticoids
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98. Kotilainen E, Hohenthal U, Karhu J, Kotilainen P: Spinal epidural lipomatosis caused by corticosteroid treatment in ulcerative colitis. Eur J Intern Med; 2006 Mar;17(2):138-40

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spinal epidural lipomatosis caused by corticosteroid treatment in ulcerative colitis.
  • Spinal epidural lipomatosis is the result of deposition of unencapsulated fat in the extradural space of the spinal canal.
  • This is the second patient with ulcerative colitis described in the literature who developed symptomatic epidural lipomatosis secondary to corticosteroid treatment.
  • All internists tending patients with chronic diseases that require corticosteroid treatment should be aware of this rare clinical entity.

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  • (PMID = 16490695.001).
  • [ISSN] 0953-6205
  • [Journal-full-title] European journal of internal medicine
  • [ISO-abbreviation] Eur. J. Intern. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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99. Raeder H, Haldorsen IS, Ersland L, Grüner R, Taxt T, Søvik O, Molven A, Njølstad PR: Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase. Diabetes; 2007 Feb;56(2):444-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase.
  • Both pancreatic volume reduction and lipomatosis have been observed in subjects with diabetes.
  • We have recently described pancreatic atrophy and lipomatosis in diabetic subjects of two Norwegian families with a novel syndrome of diabetes and exocrine pancreatic dysfunction caused by heterozygous carboxyl-ester lipase (CEL) mutations.
  • To explore the early pathological events in this syndrome, we performed radiological examinations of the pancreas in nondiabetic mutation carriers with signs of exocrine dysfunction.
  • The pancreata of nondiabetic mutation carriers exhibited increased reflectivity on ultrasound and had MRI findings indicative of lipomatosis.
  • Our findings suggest that lipomatosis of the pancreas reflects early events involved in the pathogenesis of diabetes and exocrine pancreatic dysfunction syndrome.
  • [MeSH-major] Carboxylesterase / genetics. Diabetes Mellitus / genetics. Lipomatosis / genetics. Pancreas / pathology. Pancreatic Diseases / genetics

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  • (PMID = 17259390.001).
  • [ISSN] 0012-1797
  • [Journal-full-title] Diabetes
  • [ISO-abbreviation] Diabetes
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] EC 3.1.1.1 / Carboxylesterase; EC 3.4.21.36 / Pancreatic Elastase
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100. Komagata T, Takebayashi S, Hirasawa K, Fukawa T, Arai M: Extensive lipomatosis of the small bowel and mesentery: CT and MRI findings. Radiat Med; 2007 Nov;25(9):480-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extensive lipomatosis of the small bowel and mesentery: CT and MRI findings.
  • We report a patient with extensive lipomatosis involving both the ileum and mesentery.
  • [MeSH-major] Intestine, Small. Lipomatosis / diagnosis. Magnetic Resonance Imaging. Mesentery. Tomography, X-Ray Computed
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Middle Aged

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  • (PMID = 18026907.001).
  • [ISSN] 0288-2043
  • [Journal-full-title] Radiation medicine
  • [ISO-abbreviation] Radiat Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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